Perrigo recalls infant acetaminophen grape suspension due to contaminated excipient from supplier. Products distributed by Target may be unsafe.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling infant acetaminophen grape oral suspension because it was made with a contaminated ingredient. This could pose a health risk to babies if the product is consumed.
The product was manufactured using an excipient (a substance added to the medication) that was contaminated. This contamination could lead to health issues if the product is ingested by infants.
Parents or caregivers of infants who use this specific acetaminophen suspension. Infants are most at risk due to their developing bodies.
Check for the product name 'Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle'. Products distributed by Target with NDC 11673-133-16 and batch 1CK0907 (expiring 01/31/2023) are affected.
Look for the NDC code 11673-133-16 and batch number 1CK0907 on the bottle label.
The product has been recalled due to potential contamination, so it is not safe to use.
Check for the NDC code 11673-133-16 and batch number 1CK0907 on the bottle label.
The recall does not specify a remedy, so contact Perrigo directly for guidance.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0584-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0584-2022 from Perrigo. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
