Triad Group, a manufacturer of over-the-counter products has initiated a voluntary product recall involving ALL LOTS of ALCOHOL PREP PADS, ALCOHOL SWABS, and ALCOHOL SWABSTICKS manufactured by Triad Group but which are private labeled for many accounts to the consumer level. This recall involves those products marked as STERILE as well as non-sterile products. This recall has been initiated due to concerns from a customer about potential contamination of the products with an objectionable organism, namely Bacillus cereus. We are, out of an abundance of caution, recalling these lots to ensure that we are not the source of these contamination issues.
Use of contaminated Alcohol Prep Pads, Alcohol Swabs or Alcohol Swabsticks could lead to life-threatening infections, especially in at risk populations, including immune suppressed and surgical patients. To date we have received one report of a non-life-threatening skin infection.
Alcohol Prep Pads, Alcohol Swabs and Alcohol Swabsticks are used to disinfect prior to an injection. They were distributed nationwide to retail pharmacies and are packaged in individual packets and sold in retail pharmacies in a box of 100 packets. The affected Alcohol Prep Pads, Alcohol Swabs and Alcohol Swabsticks can be identified by either “Triad Group,” listed as the manufacturer, or the products are manufactured for a third party and use the names listed below in their packaging:
Cardinal Health
PSS Select
VersaPro
Boca/ Ultilet
Moore Medical
Walgreens
CVS
Conzellin
These products were distributed in the United States, Canada and Europe.
Specific customers distributing the product and selling it at the wholesale, hospital and retail pharmacy level have been notified by certified mail with instructions on how to return the product. If a consumer has any of these types of products in their possession listing “Triad Group” as the manufacturer, they should not use the product and should return it to the place it was purchased for a full refund or call Triad Group Customer Service Monday through Friday between the hours of 8:30 A.M. and 4:00 P.M. Central Time: 262.538.2900.
DO NOT RETURN THE PRODUCT ON YOUR OWN, simply call the Triad Group Customer Service listed below and we will issue you a return authorization number and make all return arrangements.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
* Online:http://www.fda.gov/MedWatch/report.htm9
* Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: http://www.fda.gov/MedWatch/getforms.htm10 Mail to address on the pre-addressed form.
* Fax: 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food & Drug Administration.
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Friday, January 7, 2011
Triad Group Issues a Voluntary Nationwide Recall of All Lots of Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks Due to Potential Microbial Contamination
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Monday, April 6, 2009
Atico International USA Recalls Coffeemakers Sold Exclusively At Walgreens 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: Signature Gourmet(tm) 12-Cup Programmable Coffeemakers and Kitchen Gourmet(r) 10-Cup Coffeemakers
Units: About 500,000
Distributor: Atico International USA Inc., of Fort Lauderdale, Fla.
Hazard: These coffeemakers can ignite due to an electrical failure, posing a fire hazard.
Incidents/Injuries: Atico International USA, Inc. has received 23 reports of coffeemakers igniting, resulting in property damage. No injuries have been reported.
Description: This recall involves the following coffeemakers:
Name
Color
Model #
Item#
Kitchen Gourmet(r) 10-Cup Coffeemaker
White
XQ-673K
W14A3714
Signature Gourmet(tm) 12-Cup Programmable Coffeemaker
Black
XQ-673BT or CM4193D
W14A5084
The name of the coffeemaker is printed on the front of the unit. The model number and the item number are printed on a sticker located on the bottom of the unit.
Sold at: Walgreens stores nationwide: the Signature Gourmet(tm) 12-Cup programmable coffeemaker from June 2004 through March 2009 for about $20 and the Kitchen Gourmet(r) 10-Cup coffeemaker from August 2006 through December 2008 for about $10.
Manufactured in: China
Remedy: Consumers should immediately unplug and stop using the recalled coffeemaker and contact Atico International USA for instructions on returning the product for a full refund.
Consumer Contact: Consumers should call Atico International USA toll-free at (877) 546-4835 between 9 a.m. and 5 p.m. ET Monday through Friday, or visit the company's Web site at www.aticousa.com .
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Wednesday, February 4, 2009
Walgreens Recalls Café W Brand Trail Mix Containing Peanuts
Walgreens is recalling four types of Cafe W brand trail mix containing peanuts sold in most Walgreens stores. The trail mix manufacturer notified Walgreens today that the products contain peanuts from Peanut Corporation of America (PCA). PCA is the focus of the U.S. Food and Drug Administration investigation into potential salmonella contamination of peanut products. Though Walgreens is not aware of any reported cases of illness related to these products, it has issued this voluntary recall as a precautionary measure.
Walgreens has already instructed its stores to stop selling the following products:
* Walgreens Café W Marathon Mix (7 oz.), UPC 4902241012, Best By: all dates prior to 1/31/2010
* Walgreens Café W Super Energy Mix (5 oz.), UPC 4902239747, Best By: all dates prior to 8/15/2009
* Walgreens Café W Super Energy Mix (7 oz.), UPC 4902241011, Best By: all dates prior to 1/31/2010
* Walgreens Café W Cranberry Crunch (7 oz.), UPC 4902241013, Best By: all dates prior to 1/31/2010
Walgreens takes the safety of its customers seriously and is working with the FDA on this recall. For additional information, please contact Walgreens Product Quality department at 847-315-2755, Monday through Friday between 8 a.m. and 4:30 p.m. Central time. Customers who purchased the recalled products should discontinue use immediately and return items to Walgreens for an exchange or refund.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention's Website at http://www.cdc.gov.
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Tuesday, February 3, 2009
Walgreens Recalls Walgreens Brand Candy Containing Peanuts Sold From Jan. 1, 2007 To Jan. 29, 2009
Walgreens is recalling four types of Walgreens brand chocolate candy containing peanuts sold in stores from Jan. 1, 2007 to Jan. 29, 2009. The candy manufacturer notified Walgreens today that the candy contains peanuts from Peanut Corporation of America (PCA). PCA is the focus of the U.S. Food and Drug Administration investigation into potential salmonella contamination of peanut butter and paste. Though Walgreens is not aware of any reported cases of illness related to these products, it has issued this voluntary recall as a precautionary measure.
Walgreens has already instructed its stores to stop selling the following products:
* WALGREENS BRIDGE MIX 3.5 OZ, 4 OZ, 14 OZ and 15 OZ
* WALGREENS CHOCOLATE COVERED PEANUTS 3.5 OZ, 4 OZ, 13.5 OZ and 15 OZ
* WALGREENS CARAMEL NUT CLUSTERS 3.5 OZ, 4 OZ, 13.5 OZ and 15 OZ
* WALGREENS CHOCOLATE PEANUT CLUSTERS 3.5 OZ and 4 OZ
Walgreens takes the safety of its customers seriously and is working with the FDA on this recall. For additional information, please contact Walgreens Product Quality department at 847-315-2755, Monday through Friday between 8 a.m. and 4:30 p.m. Central time. Customers who purchased the recalled products should discontinue use immediately and return items to Walgreens for an exchange or refund.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody),nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention’s Web site at http://www.cdc.gov.
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Sunday, December 7, 2008
Walgreens Recalls 173 Teddy Bears With Chocolate Bars Sold Since Late September 2008
Walgreens is recalling 173 teddy bears with chocolate bars sold in stores since late September 2008. Analysis by the U.S. Food and Drug Administration found that certain samples of the chocolate provided with the teddy bears were contaminated with melamine. Customers who purchased any of the 173 teddy bears should return them immediately to the Walgreens stores where they were purchased for a full refund.
Walgreens already has instructed stores to stop selling the product, which is specifically described as an approximately 9-inch high Dressy Teddy Bear with 4-oz. Chocolate Bar. The product's UPC number is 047475864485, and the product tag also includes the item number 291332. Walgreens has not received any reports of illness or injury related to this product.
Walgreens takes the safety of its customers seriously and is working with the FDA on this recall. For additional information, visit Walgreens Web site at http://www.walgreens.com/images/pdfs/recalls/TeddyBear_Product_Safety.pdf or contact Walgreens Product Quality department at 847-315-2755, Monday through Friday between 8 a.m. and 4:30 p.m. Central time.
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