Manhattan Group Recalls Infant Rattles Due to Choking Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named
below, today announced a voluntary recall of the following consumer product.
Consumers should stop using recalled products immediately unless otherwise
instructed.

Name of Product: Tumble Tower Infant Rattles

Units: About 7,000

Manufacturer: Manhattan Group LLC, of Minneapolis, Minn.

Hazard: The blue plastic end caps of the rattle can break, resulting in small parts,
posing a choking hazard to young children.

Incidents/Injuries: Manhattan Group has received two reports of the blue plastic
end caps breaking. No injuries have been reported.

Description: The recalled Manhattan Toy(tm) baby rattle is 5 inches long and made
of clear plastic with blue end cap pieces. The two clear handles feature colorful
beads inside and brightly colored rings on the outside. A blue face spins on a
purple post inside the rattle center when it is turned.

Sold at: Gift and specialty stores nationwide, mail order catalogs, and the Internet
from September 2007 through April 2008 for about $15.

Manufactured in: China

Remedy: Consumers should take the toys away from young children and return them to
the store where purchased for a refund or contact Manhattan Group to exchange the
rattles for another toy.

Consumer Contact: For additional information, contact Manhattan Group toll-free
at (800) 541-1345 between 8 a.m. and 5 p.m. CT, Monday through Friday or visit the
firm's Web site at www.manhattantoy.com

To see this recall on CPSC's web site, including pictures of the recalled product,
please go to: http://www.cpsc.gov/cpscpub/prerel/prhtml08/08268.html

Maple Chase Co. Recalls Carbon Monoxide and Carbon Monoxide/Smoke Combo Alarms Due to Alarm Malfunction

The U.S. Consumer Product Safety Commission, in cooperation with the firm named
below, today announced a voluntary recall of the following consumer product.
Consumers should stop using recalled products immediately unless otherwise
instructed.

Name of Product: FireX Branded 10000 Series Carbon Monoxide (CO) Alarms and
12000 Series CO/Smoke Combo Alarms

Units: About 280,000

Manufacturer: Maple Chase Company, of Plain City, Ohio

Hazard: The recalled alarms can sound a "double chirp"/fault alarm in the presence
of CO, prior to going into full alarm. Upon hearing a double chirp, the Owner's
Manual instructions recommend a consumer take the alarm out of service, which
could expose consumers to hazardous levels of CO and suffer injury or death.

Incidents/Injuries: None reported.

Description: The recall includes FireX branded 10000 and 12000 series alarms with
item numbers: 10000, 12000, 12000C, 12000-6, 12200, 12220, 12400, 12400C manufactured
between June 1, 2007 and February 1, 2008. The date code appears on the back of the
unit with a four digit year, three digit month followed by the day (ex: 2007JUN1 for
June 1, 2007). Units with a manufacture date code prior to June 1, 2007 are not
included in this recall.

Sold: Commercial electrical distributors and electrical contractors and builders
for installation into new home construction. A limited number of units were sold at
Menard's nationwide from June 2007 through February 2008 for about $20 (10000 series)
and $30 (12000 series).

Manufactured in: Mexico

Remedy: Consumers should contact Maple Chase immediately to receive a free comparable
replacement alarm and make arrangements to return their recalled alarms. Consumers
should not take the alarms out of service until they receive the replacement alarm.

Consumer Contact: For more information, contact Maple Chase toll-free
at (888) 879-3906 between 8 a.m. and 6 p.m. CT Monday through Friday or go to the
firm's Web site at www.firexsafety.com

To see this recall on CPSC's web site, including pictures of the recalled product,
please go to: http://www.cpsc.gov/cpscpub/prerel/prhtml08/08267.html

Maran Inc. Children's Hooded Jackets with Drawstrings Recalled Due to Strangulation Hazard; Sold Exclusively at TJ Maxx

The U.S. Consumer Product Safety Commission, in cooperation with the firm named
below, today announced a voluntary recall of the following consumer product.
Consumers should stop using recalled products immediately unless otherwise
instructed.

Name of Product: Squeeze Kids Girl's Corduroy Jackets

Units: About 6,000

Distributor: Maran Inc., of North Bergen, N.J.

Hazard: The garments have a drawstring through the hood, which can pose a
strangulation hazard to children. In February 1996, CPSC issued guidelines (pdf)
to help prevent children from strangling or getting entangled on the neck and waist
drawstrings in upper garments, such as jackets and sweatshirts.

Incidents/Injuries: None reported.

Description: The recalled garments are brown corduroy jackets with a pink hood and
pink sequins on the front pockets. "Squeeze Kids" and style number 4JZ642FK are
printed on the care label sewn into the back collar area of the garment. The
sweatshirts were sold in girls' sizes small (7/8), medium (10), large (12/14)
and x-large (16).

Sold exclusively at: TJ Maxx retail stores nationwide during January 2007 for
about $13.

Manufactured in: China

Remedy: Consumers should immediately remove the drawstrings from the sweatshirts
to eliminate the hazard, or return the garments to the place where purchased or
to Maran Inc. to receive a refund.

Consumer Contact: For additional information, contact Maran Inc. toll-free at
(866) 431-5698 between 9 a.m. and 5 p.m. ET Monday through Friday, or visit the
firm's Web site at www.Sqz.com

To see this recall on CPSC's web site, including pictures of the recalled product,
please go to: http://www.cpsc.gov/cpscpub/prerel/prhtml08/08266.html

Atrium Initiates Voluntary Recall Action Regarding HYDRAGLIDE™ Brand Heparin-Coated Thoracic Drainage Catheters used for Autotransfusion during Cardio

Atrium Medical Corporation today (May 15, 2008) announced that it is initiating a voluntary and precautionary recall of selected lots of HYDRAGLIDE™ Brand Heparin-Coated Thoracic Drainage Catheters. Limited lots of Atrium heparin-coated Hydraglide Thoracic Catheters were manufactured with heparin found to have been contaminated with oversulfated chondroitin sulfate (OSCS). The patient risk associated with the presence of OSCS in heparin-coated medical devices is not known at this time. The U.S. Food and Drug Administration has received reports of serious injury and death in patients who have been administered injectable heparin products containing high levels of OSCS. While Atrium’s HYDRAGLIDE Catheters do not contain high levels of heparin, there still exists a potential exposure of OSCS to the patient.

Customers with affected lots are advised to immediately discontinue use of these devices and obtain replacement catheters from Atrium. Atrium will be working with our customers to replace the affected product as soon as possible. If a non-elective procedure requires use of this catheter, we recommend that you do not use the catheter with either a cell saver autotransfusion system or direct autotransfusion chest drainage collection system for cardiopulmonary bypass surgery.

Atrium has not received reports of any OSCS-related adverse events arising from any use of their Hydraglide Thoracic Catheters. This voluntary recall is being initiated as a precaution to minimize any future potential risk.

The above Customer Notification actions are being taken with the knowledge of the U.S. Food and Drug Administration. Physicians and hospital personnel with product related questions should call the company at 1-800-5-ATRIUM, Monday –Friday, 8:00 AM to 5:00 PM EST.

Sweetwater Valley Farm, Inc. Recalls Tennessee Aged Black Pepper Cheese

Sweetwater Valley Farm, Inc. of Philadelphia, TN is recalling Tennessee Aged Black Pepper Cheese because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

Tennessee Aged Black Pepper Cheese, Lot Number 616-361 was distributed in 5, 7, and 10 ounce bars through our retail store in Philadelphia, TN and a Winery in Portland, TN.

Less than 100 pounds was distributed.

This product was distributed between December 27, 2007 and May 12, 2008.

No illnesses have been reported.

The recall was the result of a routine sampling program by the Tennessee Department of Agriculture which revealed that the finished product contained the bacteria. The company has ceased the distribution of this lot as the company continues their investigation as to what caused the problem.

Consumers who have purchased lot number 616-361 of this product are urged bring it to the store for replacement or refund or ship it back to the store for replacement or refund. Contact the company’s consumer affairs department at 1-877-862-4332 for further information.

Manufacturer Removes Remaining Stocks of Trasylol

Background: On Nov. 5, 2007, the U.S. Food and Drug Administration announced that Bayer Pharmaceuticals Corp. agreed to an FDA-requested marketing suspension of Trasylol, a drug used to control bleeding during heart surgery. At that time, preliminary results from a Canadian study suggested an increased risk for death compared to two other drugs used to control bleeding.

Bayer HealthCare Pharmaceuticals Inc. has notified the FDA that the company will begin removing the remaining Trasylol stock from the U.S. market, most of which is in warehouses and hospital or physician’s stock. The FDA will work with Bayer to ensure a smooth and complete process.

Under a limited use agreement, access to Trasylol is limited to investigational use of the drug according to the procedures described in a special treatment protocol. The protocol allows treatment for certain patients who are at increased risk of blood loss and transfusions during coronary artery bypass graft surgery and who have no acceptable alternative therapy. Physicians using Trasylol in this situation must also verify that the benefits of the drug clearly outweigh the risks for their patients.

FDA limits access to certain drugs to patients with serious or immediately life-threatening disease or conditions who lack other therapeutic options and may benefit from such therapies. This type of access requires the submission of a protocol, which is reviewed and approved by the agency. Bayer has agreed to provide Trasylol through this mechanism for the limited use described above.

Trasylol is an antifibrinolytic drug approved to reduce blood loss during surgery and the need for blood transfusion in certain patient undergoing cardiopulmonary bypass in the course of coronary artery bypass graft surgery. Antifibrinolyitc drugs help slow the breakdown of blood clots and subsequent excessive bleeding.

Results from a randomized Canadian study that prompted last November’s marketing suspension of Trasylol are expected to be published this week. The data contained in this article suggest that Trasylol appears to increase the risk for death compared to two other antifibrinolytic drugs used in the study.

The findings from this randomized study are similar to those from an observational study that was discussed at a September 2007 FDA advisory committee meeting. Based upon the data available at the time, the advisory committee recommended continued marketing of Trasylol.

However, FDA requested the marketing suspension in the interest of patient safety based on the serious nature of the outcomes suggested in the preliminary data. The committee also advised that a large, randomized clinical study was needed to further assess Trasylol’s safety compared to other drugs. This recently published Canadian study helps address this need for additional information.

The FDA has not yet received full study data from the study’s researchers at the Ottawa Health Research Institute but supports Bayer’s decision to completely remove Trasylol from regular use in the U.S. market. FDA is also reviewing the available Canadian study data to reassess the currently active special treatment protocol that provides access to Trasylol.

FDA oversight requires comprehensive and thorough studies of a drug not only during the pre-market review phase but throughout the drug’s life cycle. As studies and data on Trasylol emerged over the years, FDA actions included labeling changes, safety communications to physicians and other health care professionals, public discussion and review of study data at two Advisory Committee meetings, as well as close scrutiny of the ongoing studies.

The agency will consider a variety of study designs to support the review process for future antifibrinolytics, and will incorporate into these considerations information from the recently published Canadian study. FDA will continue to publicly disseminate safety information.

Medtronic Initiates Voluntary Field Actions for Selected Heparin-Coated Products Used During Cardiopulmonary Bypass

Medtronic, Inc. today (May 7, 2008) announced that it is initiating a voluntary and precautionary recall of selected products featuring the Carmeda BioActive surface. The affected devices are disposable products used during cardiopulmonary bypass (CPB) for heart surgeries. Affected products include blood oxygenators, reservoirs, pumps, cannulae, and tubing packs. This action is being taken subsequent to the U.S. Food and Drug Administration's April 8, 2008 recommendation to device manufacturers that heparin supplies be checked with newly-developed tests, and that affected products be evaluated for possible field corrective action.

Limited lots of Carmeda-coated products were manufactured with heparin found to have been contaminated with oversulfated chondroitin sulfate (OSCS). The patient risk associated with the presence of OSCS in heparin-coated medical devices is not known at this time. However, the U.S. Food and Drug Administration has received reports of serious injury and death in patients who have been administered injectable heparin products containing high levels of OSCS.

Medtronic has not received reports of any OSCS-related adverse events arising from the use of Carmeda CPB products. It is unclear, however, if exposure to Carmeda-coated medical devices, made with comparatively small amounts of heparin, could cause adverse events similar to those observed with injectable heparin formulations. As a result, Medtronic has initiated a precautionary recall of affected Carmeda products.

In a separate action, Medtronic is advising customers that selected lots of Trillium-coated products were also manufactured with heparin containing OSCS. Trillium is another biosurface used on CPB products. The amount of heparin on the product is significantly lower than that contained on the Carmeda product. Medtronic's ultimate goal is to remove contaminated products from the market. However, based on the current data, the benefit of using the affected products outweighs any potential risk to patients. Since the maximum possible patient exposure to heparin from Trillium is extremely low, customers can continue to use the affected Trillium products until a replacement is available.

The above actions are being made with the knowledge of the U.S. Food and Drug Administration. Patients with questions should talk to their physician. Physicians or Pefusionists with medical questions related to Medtronic therapies should contact Medtronic at 1-800-638 0218, Monday – Friday, 8:00 a.m. to 5:00 p.m. CDT

Air Pistols That Can Fire Unexpectedly Are Recalled by Umarex USA

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below
today announced a voluntary recall of the following consumer product. Consumers
should stop using recalled products immediately unless otherwise instructed.

Name of Product: Air Pistols

Units: About 7,250

Distributor: Umarex USA Inc., of Fort Smith, Ark.

Manufacturer: DianaWerk GmbH & Co., of Rastatt, Germany

Hazard: The air pistols can accidentally discharge, posing a risk of serious injury
if the air pistol is loaded and pointed at the user or another person when it
discharges.

Incidents/Injuries: Umarex USA has received one report of an injury involving the
recalled air pistols. The pistol reportedly fired a pellet unexpectedly and struck
the user in the lower leg causing swelling.

Description: The recall involves the RWS-5G Magnum Air Pistol. The air pistols,
which are used for target and recreational shooting, use spring air to fire pellets.
The air pistols are black and measure 17 ¾ x 6 inches. "RWS Diana P5 Magnum" is
printed on the top of the air pistol. Serial numbers 03316930 through 03344312 are
included in this recall and are stamped on the left side of the air pistol's barrel.

Sold by: Sporting goods stores and gun shops nationwide from July 2006 through
February 2008 for about $250.

Manufactured in: Germany

Remedy: Consumers should immediately stop using the recalled air pistols and
contact Umarex USA to receive instructions on returning the air pistol for a free
repair. Umarex USA has contacted known purchasers of the air pistol. Consumers who
have not received direct notification should contact Umarex USA immediately.

Consumer Contact: For additional information, contact Umarex USA toll-free at
(866) 633-2910 anytime, or visit the firm's Web site at www.umarexusa.com

To see this recall on CPSC's web site, including pictures of the recalled product,
please go to: http://www.cpsc.gov/cpscpub/prerel/prhtml08/08265.html

Baby Bottle and Food Warmers Recalled by Munchkin Due to Fire Hazard

The U.S. Consumer Product Safety Commission, in
cooperation with the firm named below, today announced a voluntary
recall of the following consumer product. Consumers should stop using
recalled products immediately unless otherwise instructed.

Name of Product: Deluxe Bottle and Food Warmers

Units: About 5,000

Manufacturer: Munchkin Inc., of North Hills, Calif.

Hazard: The bottle and food warmers can overheat, posing a fire hazard.

Incidents/Injuries: Munchkin has received nine reports of units
overheating, several of which ignited, causing damage to countertops. No
injuries have been reported.

Description: This recall involves the Munchkin Deluxe Bottle and Food
Warmer with Pacifier Cleaning Basket 2-in-1 Design, model #13301 and lot
number TP-1487. The product is used to warm food and bottles of various
sizes. The set includes a main basket, a lift-out basket, an adapter
ring, and a measuring cup. "Munchkin" is located on the front of the
warmer and "TP-1487" is located on the bottom. Only warmers bearing lot
number "TP-1487" are included in this recall.

Sold at: Various retailers nationwide and company's catalog from June
2007 through April 2008 for about $20.

Manufactured in: China

Remedy: Consumers should stop using bottle and food warmers with lot
number TP-1487 immediately and contact Munchkin to receive a free
replacement.

Consumer Contact: For additional information, contact customer service
toll-free at (866) 619-8673 between 9 a.m. and 5 p.m. PT Monday through
Friday, or visit the firm's Web site at www.munchkin.com

To see this recall on CPSC's web site, including pictures of the
recalled product, please go to:
http://www.cpsc.gov/cpscpub/prerel/prhtml08/08263.html

Blount Fine Foods Issues Allergy Alert On Undeclared Shrimp in All Natural New England Clam Chowder, 20 Oz Cup

Blount Fine Foods of Fall River, MA is recalling Blount All Natural New England Clam Chowder, Net Wt. 20 oz with Lot: 0424086D, Sell by date: 6/23/2008, because it may contain undeclared shrimp. People who have an allergy or severe sensitivity to shrimp run the risk of serious or life-threatening allergic reaction if they consume these products. Our firm has recovered 1,400 of 1,416 units produced, 16 units are in distribution.

Blount New England Clam Chowder was distributed through the following supermarket chains: Shaw's Supermarkets (in Massachusetts and Connecticut), Omni Foods (in Weston, MA), Donelan Market (in Acton and Littleton, MA), and The Cirelli Marketplace store (Middleboro, MA). The product is identified as a 20oz plastic cup with a film seal and plastic lid. The dark blue product label reads: Blount Signature Soups All Natural New England Clam Chowder, Keep Refrigerated. The lot code and sell by date are printed in black ink on the bottom of the cup.

No illnesses have been reported to date. The recall was initiated after it was discovered that product containing shrimp was distributed in packaging that did not reveal the presence of shrimp. Subsequent investigation indicates the problem was caused by an isolated, temporary breakdown in the company's production and packaging processes.

Consumers who have purchased Blount All Natural New England Clam Chowder are urged to return it to the place of purchase for a full refund. Consumers who have health-related concerns should contact their physician. Consumers with questions may contact the company at 1-800-274-2526.

TJ Power Sports Recalls Dune Buggies Due To Ejection Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named
below,today announced a voluntary recall of the following consumer product.
Consumers shouldstop using recalled products immediately unless otherwise
instructed.

Name of Product: Twister Hammerhead Dune Buggies

Units: About 400

Importer: TJ Power Sports LLC, of Irving, Texas

Hazard: The seat belt adjustment for the shoulder buckle can break during impact
or stress, posing an ejection and injury hazard to driver and passenger.

Incidents/Injuries: TJ Power Sports has received one report of a seat belt
breaking that resulted in nerve damage to the rider's right arm.

Description: This recall involves the dune buggies "Twister Hammerhead" with model
number UM150IIR and model year 2004. The dune buggies were available in red, blue,
or green. "Twister Hammerhead", the model number, and the model year can be found
imprinted on the bar behind the driver and passenger seats.

Sold through: Twister dealers nationwide and online retailers from July 2004
through December 2004 for about $3,000.

Manufactured in: China

Remedy: Consumers should stop using these dune buggies immediately and contact
TJ Power Sports for instructions on how to receive a replacement seat belt.

Consumer Contact: For additional information, visit the firm's Web site
www.tjpowersports.com

To see this recall on CPSC's web site, including a picture of the recalled
product,please go to:
http://www.cpsc.gov/cpscpub/prerel/prhtml08/08262.html

Updated: Lezza Blue Raspberry Italian Ice Recalled

RR Note: Please note several additional states, including Georgia, have been added to the list.

Cedar Crest Specialties, Inc., Manitowoc, Wisconsin announced on Friday, May 2nd 2008 a recall on one lot code of Lezza Blue Raspberry Italian Ice because, it may contain milk allergen protein that is not listed in the product’s ingredient statement. People who have an allergy or severe sensitivity to milk may experience a potentially serious or life-threatening allergic reaction if they consume this product.

The product is in round plastic pint containers with a lot code of 2116. Blue Raspberry is the flavor of the product.

The product was distributed to retail outlets in Illinois, Wisconsin, Oklahoma, Texas, Michigan, Louisiana, Kansas, Indiana, Georgia, Florida, Ohio, Missouri, Kentucky, Nebraska, Pennsylvania, Arkansas, and Minnesota during 2006 and 2007.

There is no health risk for consumers who are not allergic to milk.

No other Lezza Italian Ice products are included in this recall. The product is flavored frozen water ice and must be kept frozen.

There is one reported allergic reaction attributed to this product. After customer reported allergic reaction, product in customer’s possession was retrieved and sent to independent lab for analysis. Unopened product was also sent to independent lab for testing. Decision for recall was reached after lab tests were completed. Only one complaint was filed about lot code 2116.

Concerned consumers are encouraged to return any affected product to the place of purchase to receive a full refund. Consumers with questions or concerns may contact Cedar Crest Specialties, Inc. at 1-866-233-2788.

Hydrox Labs Issued a Voluntary Recall of Alcohol-Free Mouthwash Nationwide Distributed by Cardinal Health

Hydrox Labs, Elgin, IL has issued a voluntary recall of Cardinal Health labeled alcohol-free mouthwash. As a result of this recall, Cardinal Health is initiating a voluntary recall of the same alcohol-free mouthwash. The FDA has been apprised of the action. The mouthwash has been tested and been found positive for Burkholderia cepacia (B. cepacia). The CDC has confirmed hospital illnesses in one state associated with the use of the affected mouthwash.

Product was distributed to hospitals, medical centers, and long term care facilities nationwide.

B. cepacia poses little medical risk to healthy people. However, people who have certain health problems such as weakened immune systems or chronic lung diseases, particularly cystic fibrosis (CF), may be more susceptible to infections with B. cepacia. B. cepacia is a known cause of infections in hospitalized patients. B. cepacia bacteria are often resistant to common antibiotics. The effects of B. cepacia on people vary widely, ranging from no symptoms at all, to serious respiratory infections, especially in patients with CF.

The recall includes the following products:

Description	Reorder Number
Alcohol-Free Mouthwash, Cardinal Health, 4 oz.	AG-210

Product lot number 26228 is affected. Affected product can be identified by checking the lot code stamped on the Cardinal Health label. The Lot number is located on the side of the bottle.

The mouthwash may also be found in certain Personal Hygiene Hospital Admission Kits. If you received mouthwash labeled for Cardinal Health from your healthcare provider, please check to see if the reorder number on the label matches the recalled reorder numbers listed above, then check to see if the lot number matches the recalled lot number.

Customers who have Cardinal Health labeled alcohol free mouthwash which is being recalled should stop using the product and contact Cardinal Health for instructions.

Cardinal Health is notifying their customers via overnight mail and is arranging for all product to be returned for credit.

Onward Manufacturing Recalls Gas Grills Due to Fire and Burn Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below,
today announced a voluntary recall of the following consumer product. Consumers should
 stop using recalled products immediately unless otherwise instructed.

Name of Product: Broil King Gas Grills

Units: About 4,800

Manufacturer: Onward Manufacturing Co., of Ontario, Canada

Hazard: The bottom of the cook box that contains the burners can melt or crack as a
result of a grease fire. This poses a fire and burn hazard to consumers.

Incidents/Injuries: None reported

Description: This recall includes the Signet, Sovereign and Sovereign XL series gas
grills.

Signet series: (model #'s starting with 986xxx) 400 sq. inch cooking surface with
3 burners and drop-down shelves; includes models with side and rear burners

Sovereign series: (model #'s starting with 987xxx) 450 sq. inch cooking surface with
3 burners and drop-down shelves; includes models with side and rear burners.

Sovereign XL series: (model #'s starting with 988xxx) 600 sq. inch cooking surface
with 4 burners and drop-down shelves.

The model number can be located on the back panel of the grill.

Sold at: Independent retailers nationwide from February 2006 through April 2008 for
between $450 and $700.

Manufactured in: Canada

Remedy: Consumers should stop using the grill immediately and contact Onward
Manufacturing for a free repair kit.

Consumer Contact: For further information, visit the firm's Web site
at www.broilkingbbq.com or call toll-free at (866) 434-7455 between 8:30 a.m. and
5 p.m. PT Monday through Friday.

Lezza Blue Raspberry Water Ice Recalled from Three Midwestern States

Cedar Crest Specialties, Inc. today announced a recall on one lot code of Lezza Blue Raspberry Water Ice in round plastic pint containers with a lot code of 2116 because it may contain undeclared milk protein. The product was distributed to retail outlets in Illinois, Wisconsin, and Minnesota during 2006 and 2007.

The product is being recalled because it may contain milk allergen protein that is not listed in the product’s ingredient statement. People who have an allergy or severe sensitivity to milk may experience a potentially serious or life-threatening allergic reaction if they consume this product.

There is no health risk for consumers who are not allergic to milk.

No other Lezza water ice products are included in this recall.

There is one reported allergic reaction attributed to this product.

Concerned consumers are encouraged to return any affected product to the place of purchase to receive a full refund. Consumers with questions or concerns may contact Cedar Crest Specialties, Inc. at 1-866-233-2788.