FDA Drug Recalls

Recalls / Class II

Class IID-0591-2022

Product

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by Target Corp., Minneapolis, MN 55403 NDC: 11673-130-26

Brand name
Up And Up Childrens Acetaminophen
Generic name
Acetaminophen
Active ingredient
Acetaminophen
Route
Oral
NDC
11673-130
FDA application
M013
Affected lot / code info
Batch: 1CK1146, Exp 02/28/2023

Why it was recalled

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Recalling firm

Firm
Perrigo Company PLC
Manufacturer
Target Corporation
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
515 Eastern Ave, Allegan, Michigan 49010-9070

Distribution

Quantity
26,832 bottles
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2021-10-26
FDA classified
2022-02-23
Posted by FDA
2022-03-02
Terminated
2023-09-29
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0591-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: Up And Up Childrens Acetaminophen · FDA Drug Recalls