Perrigo recalls strawberry-flavored acetaminophen liquid for children due to contaminated excipient. Affected bottles have NDC 0363-0971-26 and batch numbers 1DK0917 or 1GK0905. Stop using immediately if you have this product.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling a specific children's acetaminophen liquid because it was made with a contaminated ingredient. This could cause health issues if the product is used as intended. The recall affects bottles sold with certain batch numbers and distribution dates.
The product was made using an excipient (a substance added to the liquid) that was contaminated. This contamination could lead to health problems if the product is consumed by children. The exact health risk is not specified in the recall notice.
Children who use this acetaminophen liquid are most at risk. Parents or caregivers who purchased the product from Walgreen stores or online are likely affected.
Check the bottle label for 'Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL)'. Look for NDC code 0363-0971-26 and batch numbers 1DK0917 or 1GK0905.
Discard the product if you have it, as it contains a contaminated ingredient that could cause health issues.
The product was manufactured with a contaminated excipient that was recalled from the supplier, posing a potential health risk.
Batch numbers 1DK0917 and 1GK0905 are affected, with an expiration date of January 31, 2023.
Look for the NDC code 0363-0971-26 and batch numbers 1DK0917 or 1GK0905 on the bottle label.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0583-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0583-2022 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.
