Archive | Infant drug recall RSS feed for this section

Infant Acetamenophin Sold by Local Retailers Recalled

3 Nov

 

Walgreens, Kroger, Meijer and Babies R Us brands are among the listed batches of infant acetamenophin recalled today by manufacturer Perrigo.  The Kroger brand is sold locally at Food4Less stores.  While the product does not appear to be defective, the recall notice was issued because some packages may contain unmarked syringes.  The company warns that unmarked dosing syringes should not be used.  If you have a product that has dosage markings on the syringe, it is perfectly safe to use according to the release.  The complete list of brands and lot numbers is:

Label Batches
BABIES R US 3KK0606
CARE ONE 3HK0564
EQUALINE 3HK0672
EQUATE 3HK0672, 3JK0433, 3JK0594, 3JK0595, 3JK0653, 3JK0673, 3KK0815, 3KK0817
HARMON FACE VALUES 3JK0594
HEALTH MART 3HK0671
HEALTHY ACCENTS 3HK0671, 3KK0606
HEB 3KK0606
KROGER 3GK0645, 3GK0704, 3HK0671, 3JK0433, 3JK0595, 3JK0653, 3JK0433, 3JK0595, 3GK0645, 3GK0704, 3JK0595
LEADER DRUG 3JK0433, 3JK0594
MEIJER 3JK0594, 3JK0597
PUBLIX 3JK0595
RITE AID 3GK0704
TOPCARE 3KK0359, 3KK0494
UP & UP 3HK0672
WALGREEN 3GK0704, 3HK0564, 3HK0671, 3JK0433, 3JK0595, 3JK0610, 3KK0360

In a statement, the company said:

The Perrigo Company (NYSE: PRGO; TASE) announced today that it has initiated a voluntary, nationwide product recall to the retail level of 18 batches of its acetaminophen infant suspension liquid, 160 mg/5 mL, sold in 2 oz. and 4 oz. bottles with syringes in a box under the store brand products listed below above. The recall is being initiated because of the remote potential that a small number of packages might contain an oral dosing syringe without dose markings. The correct syringe should have a white or yellow plunger with specific dose markings for 1.25 mL, 2.5 mL, 3.75 mL, and 5 mL. If the product’s syringe has these dose markings, consumers can continue to use the product while following labeled use instructions.

Using an oral syringe without dose markings can result in inaccurate dosing, especially in infants who could mistakenly get too high a dose.

Commenting on this market action, Perrigo’s Chairman, President and CEO Joseph C. Papa stated, “There are no issues or concerns with respect to the safety or efficacy of the product, only the potential that the oral dosing device in a relatively small number of packages could be unmarked. Out of an abundance of caution, we are taking this measure to maintain the highest possible product quality standards for our retail customers and consumers. While we cannot be certain that any of these unmarked dosing devices were released into our customers’ supply chains, taking this action is the right thing to do.” Perrigo has not received any reports or complaints related to this defect nor have they found any product with missing dose markings on re-examination of product on hand.

This OTC product is indicated for the relief of fever and minor aches and pains and can be used in infants, children and adults. These recalled products are sold by distributors nationwide and distributed through retail stores.

Perrigo is notifying its distributors and customers by verbal and e-mail communication today, followed by formal FedEx-delivered communication. It also is arranging for return of all recalled products. Distributors/retailers that have the acetaminophen infant suspension liquid that is being recalled should stop distribution and return product.

If the oral dosing device contained in the package has dose markings, no action is required, and the consumer can continue to use the product consistent with the label instructions. If the package contains an oral dosing device that does not have dose markings, the consumer should not use the product and should call Perrigo’s Consumer Affairs Department, toll free, 1-800-719-9260. Consumers should contact their physician or healthcare provider if they have any questions, or if they or their children experience any problem that could possibly be related to this drug product.

Adverse events that may be related to the use of this product may be reported to FDA’s MedWatch Adverse Event Reporting Program either online, by regular mail or by fax:

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Advertisements