Perrigo recalls nasal spray due to contaminated excipient from supplier. Products distributed by Walmart may pose health risks. Consumers should check NDC codes and batch numbers for affected items.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling a nasal decongestant spray because it was made with a contaminated ingredient. This could cause health issues if used, so affected consumers should stop using it and contact the company for a replacement.
The nasal spray was made using an ingredient that was contaminated during manufacturing. This contamination could cause health problems if the product is used, but the specific risks are not detailed in the recall notice.
People who own or use the Perrigo No Drip Nasal Spray with NDC 49035-388-10 and batch numbers 1CK0897, 1FK1233, 1FK1232 (expiring 01/31/2023) are affected. Those with allergies or sensitive health conditions may be at higher risk.
Check for the NDC code 49035-388-10 and batch numbers 1CK0897, 1FK1233, or 1FK1232 on the product label. The product was distributed by Walmart and expires by January 31, 2023.
Look for the NDC code 49035-388-10 and batch numbers 1CK0897, 1FK1233, or 1FK1232 on the label.
Reach out to Perrigo for a replacement or refund if you have the recalled product.
The recall states the product was made with a contaminated ingredient, so it is not safe to use. Consumers should stop using it and contact Perrigo for a replacement.
Check the product label for NDC code 49035-388-10 and batch numbers 1CK0897, 1FK1233, or 1FK1232. The product was distributed by Walmart and expires by January 31, 2023.
Contact Perrigo for a replacement or refund. Do not use the product if you have the recalled batch numbers.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0626-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0626-2022 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.
