Perrigo recalls Sinus Severe nasal decongestant due to contaminated excipient from supplier. Affected bottles have specific NDC and batch numbers. Consumers should check labels and contact Perrigo for details.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling Sinus Severe nasal decongestant bottles that were made with a contaminated ingredient. This could pose a health risk if the contaminated ingredient is absorbed by the body.
The product was manufactured using an excipient (a substance added to the product) that was contaminated by the supplier. This contamination could cause health issues if the product is used as intended.
People who own or use Sinus Severe nasal decongestant bottles with the specific NDC and batch numbers listed in the recall. Those with allergies to the ingredients may be at higher risk.
Check the label for the product name 'Sinus Severe', 1 fl oz (30 mL) per bottle, and the NDC number 55910-696-10. Also look for batch numbers 1BK0931 (exp 12/31/2022), 1CK0900 (exp 01/31/2023), or 1HK1196 (exp 02/28/2023).
Look for the NDC number 55910-696-10 and batch numbers 1BK0931, 1CK0900, or 1HK1196 on the bottle.
The product was manufactured with a contaminated excipient, which could pose a health risk. Consumers should check if they have the recalled bottles and follow the recall instructions.
Check the label for the NDC number 55910-696-10 and batch numbers 1BK0931 (exp 12/31/2022), 1CK0900 (exp 01/31/2023), or 1HK1196 (exp 02/28/2023).
The recall does not specify a remedy, so contact Perrigo directly for instructions 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-0627-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0627-2022 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.
