Perrigo recalls Severe Congestion Nasal Spray with contaminated ingredients due to CGMP deviations. Affected products have specific NDC and batch numbers. Consumers should contact the manufacturer for details.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling a nasal spray product because it was made with contaminated ingredients. This could pose a health risk to users, so affected consumers should stop using it and contact the manufacturer for instructions.
The nasal spray 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 used, though the exact risk level isn't clearly stated in the recall notice.
People who own or use the recalled Severe Congestion Nasal Spray with the specific NDC and batch numbers listed in the recall notice are affected. Those with the product may be at risk if they have health conditions that make them more sensitive to contaminants.
Check the product label for the NDC number 21130-813-10 and batch numbers 1BK0716 (expiring 12/31/2022) or 1FK1251, 1HK1196 (expiring 02/28/2023). The product was distributed by Better Living Brands LLC.
Look for the NDC number 21130-813-10 and batch numbers 1BK0716, 1FK1251, or 1HK1196 on the label.
The recall notice states the product was made with contaminated ingredients, so it is not safe to use. Affected consumers should stop using it.
Check the product label for the NDC number 21130-813-10 and batch numbers 1BK0716 (expiring 12/31/2022) or 1FK1251, 1HK1196 (expiring 02/28/2023).
The recall notice does not specify a remedy, so contact the manufacturer for instructions on what to do next.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0609-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0609-2022 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.
