Perrigo Company PLC recalls bubblegum-flavored children's acetaminophen suspension after finding contaminated ingredients in the manufacturing process. This affects specific batches sold through Walmart. Consumers should check product labels for batch numbers and expiration dates.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling bubblegum-flavored children's pain and fever syrup because it was made with contaminated ingredients. This could pose a health risk to children who take the product, especially if the contamination leads to illness or injury.
The syrup was manufactured using an excipient (a substance added to the product) that was contaminated. This contamination could lead to health issues if the product is consumed by children, though the exact risk is not specified in the recall notice.
Children who use this specific syrup are at risk. Parents and caregivers who purchased the product through Walmart stores are most likely affected.
Check the product label for the batch numbers 1BK0784 (expiring 12/31/2022) or 1CK0997 and 1CK1083 (expiring 01/31/2023). The product was sold through Walmart stores.
Look for batch numbers 1BK0784 (expiring 12/31/2022) or 1CK0997 and 1CK1083 (expiring 01/31/2023) on the bottle.
The recall states the product was made with contaminated ingredients, but the exact health risk is not specified. Do not use the product until you confirm it's not affected.
Check the product label for batch numbers 1BK0784 (expiring 12/31/2022) or 1CK0997 and 1CK1083 (expiring 01/31/2023).
The recall does not specify a remedy, so contact Perrigo directly for guidance on safe disposal or alternatives.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0580-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0580-2022 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.
