Perrigo recalls child acetaminophen strawberry suspension due to contaminated excipient from supplier. Products distributed by Target may pose health risks. Check NDC 11673-759-26 and batch numbers for affected items.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling child acetaminophen strawberry oral suspension bottles that were manufactured with a contaminated ingredient. This could pose a health risk to children using the product.
The product was made using an excipient (a substance added to the medication) that was contaminated by the supplier. This contamination could potentially cause health issues if the product is ingested by a child.
Children who use the recalled acetaminophen suspension are at risk. Parents and caregivers of children using this product should check if they have the affected bottles.
Check for the NDC code 11673-759-26 and batch numbers 1FK1252 or 1GK0905 on the bottle. The product was distributed by Target and expires January 31, 2023.
Look for NDC 11673-759-26 and batch numbers 1FK1252 or 1GK0905 on the bottle label.
The product was manufactured with a contaminated excipient that could pose health risks, so it is not safe to use.
Check for NDC 11673-759-26 and batch numbers 1FK1252 or 1GK0905 on the bottle label.
The official 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-0594-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0594-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.