Perrigo recalls No Drip Nasal Mist due to contaminated excipient from supplier. Products distributed by CVS may pose health risks. Consumers should check NDC 59779-388-10 and batch 1FK1164.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling No Drip Nasal Mist nasal decongestants because they were made with a contaminated ingredient. This could lead to health issues if the product is used. Consumers should stop using affected products and contact CVS for details.
The nasal decongestant was manufactured using an excipient (ingredient) that was contaminated by the supplier. This contamination could cause health problems when the product is used, though the specific risks are not clearly stated in the recall.
People who own or use the recalled No Drip Nasal Mist nasal decongestant (1 FL Oz bottles) distributed by CVS. Those with allergies or sensitive health conditions may be at higher risk.
Check for the NDC code 59779-388-10 and batch number 1FK1164 on the product label. The product was distributed by CVS Pharmacy, Inc., and sold between the dates listed on the expiration.
Look for the NDC code 59779-388-10 and batch number 1FK1164 on the product label.
The recall states the product was made with a contaminated excipient, which could pose health risks. The official notice does not specify the exact risks or safe usage conditions.
The recall record does not mention any remedy or replacement options.
The recall record does not specify a remedy, so the official notice does not provide 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-0615-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0615-2022 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.
