Perrigo recalls cherry-flavored acetaminophen liquid due to contaminated excipient from supplier. Products distributed by Walmart with NDC 49035-959-26 batch 1BK1045. Stop using immediately to avoid potential health risks.
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 from a supplier. This could pose a health risk if the product is used, so affected consumers should stop using it immediately.
The product was manufactured using an excipient (a substance used in the production process) that was contaminated. This contamination could lead to health issues if the product is consumed by children.
Parents or caregivers who purchased this acetaminophen liquid for children are most at risk. The product was sold through Walmart stores and online.
Check for the product name 'Acetaminophen Child Dye Free Cherry Flavor Oral Suspension' with NDC code 49035-959-26 and batch number 1BK1045. Products were distributed by Walmart and sold between the time of production until December 31, 2022.
Immediately stop using the recalled acetaminophen liquid product 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.
The NDC number is 49035-959-26.
Check for the product name 'Acetaminophen Child Dye Free Cherry Flavor Oral Suspension' with NDC code 49035-959-26 and batch number 1BK1045.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0589-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0589-2022 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.
