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Back Home Recall Medications Perrigo Acetaminophen Infant Suspension Liquid Recall

Perrigo Acetaminophen Infant Suspension Liquid Recall

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Recalled - Acetaminophen infant suspension liquid

 

 

 

This recall is being issued by: Food and Drug Administration
Recalled on: November 2, 2013

Description: Perrigo recalls18 batches of its acetaminophen infant suspension liquid, 160 mg/5 mL, sold in 2 oz. and 4 oz. The oral dosing syringes do not have dose markings which can result in inaccurate dosing, especially in infants who could mistakenly get too high a dose.

Bottles with syringes are sold under various store brands. The following brands and batches are involved in this recall:
 
 
 
 
 

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

Have this product?: If the oral dosing device contained in the package has dose markings (for 1.25 mL, 2.5 mL, 3.75 mL, and 5 mL), then no action is needed. If oral dosing device does not have dose markings, the FDA is recommending that you immediately stop using the recalled product and contact Perrigo’s Consumer Affairs Department at 800-719-9260.

To learn more on this recall visit: FDA's website

The recall presented here has been obtained directly from the U.S. Food and Drug Administration (FDA) is a division of the Department Health and Human Services and is responsible for monitoring medications, biological products, medical devices, food, cosmetics, and products that emit radiation.

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