Perrigo recalls cherry-flavored acetaminophen liquid due to contaminated excipient from supplier. Products may pose health risks if ingested. Check NDC 30142-818-26 batch 1BK1045.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling cherry-flavored acetaminophen liquid because it was made with a contaminated ingredient. This could cause health issues if the product is used as intended.
The product was made using an excipient (a substance added to the medication) that was contaminated. This contamination could lead to health problems if the product is consumed.
Parents and caregivers of children who own this specific acetaminophen liquid. Children are at higher risk due to the product's intended use.
Check for the NDC code 30142-818-26 and batch number 1BK1045 on the bottle. The product is a 4 fl oz (118 mL) cherry-flavored acetaminophen liquid.
Look for NDC 30142-818-26 and batch 1BK1045 on the bottle label.
The product may pose health risks due to contamination, so it is not safe to use as intended.
Check for NDC 30142-818-26 and batch 1BK1045 on the bottle label.
The recall record 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-0588-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0588-2022 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.
