Perrigo recalls nasal spray with contaminated ingredient from supplier. Products may pose health risks due to impurities in manufacturing. Consumers should check product details and follow official recall instructions.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling nasal sprays that were made with a contaminated ingredient. This could pose health risks to users, so affected consumers should stop using the product and contact the company for guidance.
The nasal spray was manufactured using an excipient (a substance added to the product) that was contaminated during production. This contamination could lead to health issues if the product is used, though the exact risk level is not specified in the recall.
People who own or use the Perrigo Severe Congestion Nasal Spray with the specific NDC code 41163-343-10 and batch number 1FK1251 are affected. Those with allergies to the ingredients or sensitive health conditions may be at higher risk.
Check for the product name 'Severe Congestion Nasal Spray, No Drip Plus Menthol' with NDC code 41163-343-10 and batch number 1FK1251. The product was distributed by SuperValu in the US and expired February 28, 2023.
Look for the NDC code 41163-343-10 and batch number 1FK1251 on the product label.
The recall states the product was made with a contaminated ingredient, so it is not safe to use. Perrigo recommends stopping use and following the recall instructions.
Check for the NDC code 41163-343-10 and batch number 1FK1251 on the product label. The product was distributed by SuperValu in the US and expired February 28, 2023.
The recall does not specify a remedy, so contact Perrigo directly for guidance on what to do with the product.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0610-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0610-2022 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.
