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Class II · ModerateRecall completed

Up And Up Acetaminophen

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberBatch: 1CK0907, Exp 01/31/2023
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byTarget Corporation
Brand nameUP AND UP ACETAMINOPHEN
Generic nameACETAMINOPHEN
Active ingredient(s)ACETAMINOPHEN
Distributed by / forTarget Corporation, Minneapolis, MN 55403
NDC11673-133-16
Show the full FDA record
Full product labelAcetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, Distributed by Target Corporation, Minneapolis, MN 55403. NDC: 11673-133-16
Recalling firmPerrigo Company PLC
DistributionNationwide in the USA
Quantity22,140 bottles
Recall initiated2021-10-26
Report date2022-03-02
Recall completed2023-09-29
Recall numberD-0584-2022
ClassificationClass II
FDA statusTerminated
Origin on fileAllegan MI United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.