Perrigo recalls nasal spray with contaminated ingredients due to CGMP deviations. Products may contain unsafe excipients from a supplier recall. Consumers should check NDC numbers and batch dates for affected items.
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 poses a risk of harm from unsafe substances in the product.
The nasal spray was manufactured using an excipient (ingredient) that was recalled by the supplier due to contamination. This means the product could contain harmful substances that might cause health issues when used.
People who own or use the recalled nasal spray products are affected. Those with sensitive health conditions may be at higher risk due to potential contamination.
Check for the NDC number 55910-511-10 and batch numbers 1BK0716 (exp 12/31/2022), 1CK0899 (exp 01/31/2023), or 1FK1163 (exp 01/31/2023). The product is sold by DolgenCorp, LLC in Goodletttsville, TN.
Look for the NDC number 55910-511-10 and batch numbers 1BK0716, 1CK0899, or 1FK1163 on the product label.
The recall states the product was made with contaminated ingredients, so it is not safe to use. The manufacturer recommends checking the NDC and batch numbers for affected items.
The recall does not specify a remedy, so you should check the product details and contact the manufacturer if you have concerns.
Check for the NDC number 55910-511-10 and batch numbers 1BK0716 (exp 12/31/2022), 1CK0899 (exp 01/31/2023), or 1FK1163 (exp 01/31/2023) on the product label.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0606-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0606-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
