Perrigo recalls nasal spray with contaminated ingredients from a supplier. Products may pose health risks due to impurities in the manufacturing process. Consumers should check product details and contact Perrigo for guidance.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling nasal sprays that were made with contaminated ingredients. This could pose health risks to users, especially those with sensitive systems or pre-existing conditions.
The spray was manufactured using an excipient (ingredient) that was recalled by the supplier due to contamination. This contamination could lead to health issues when the product is used, though the exact risk level isn't specified in the recall notice.
People who own or use the recalled nasal spray products are affected. Those with compromised immune systems or existing health conditions may be at higher risk.
Check for the product name 'Severe Congestion Nasal Spray, No Drip Plus Menthol' with NDC 41520-108-10 (Batch 1BK0716, Exp 12/31/2022) or NDC 41520-108-11 (Batch 1FK1251, Exp 02/28/2023).
Look for the NDC codes 41520-108-10 or 41520-108-11 on the product label.
The recall states that the product was manufactured with a contaminated excipient, but specific health risks are not detailed in the notice.
Check the product label for NDC codes 41520-108-10 (Batch 1BK0716, Exp 12/31/2022) or 41520-108-11 (Batch 1FK1251, Exp 02/28/2023).
The recall does not specify a remedy, so contact Perrigo directly for guidance on next steps.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0607-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0607-2022 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.
