Perrigo Company recalls Maximum Strength No Drip Nasal Spray (1 fl oz) manufactured with contaminated excipients. Products distributed by Rite Aid with specific NDC and batch numbers. Consumers should check labels and contact Rite Aid for details.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling Maximum Strength No Drip Nasal Sprays that were made with contaminated ingredients. This could pose a health risk if the contaminated material enters the body through nasal use.
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 as intended.
People who own or use the recalled nasal spray bottles labeled with NDC 11822-6319-1 and batch numbers 1BK0964 or 1FK1164 (expiring January 31, 2023) are affected. Those using the product for nasal congestion relief are most at risk.
Check for the product name 'Maximum Strength No Drip Nasal Spray' on the label. Look for NDC code 11822-6319-1 and batch numbers 1BK0964 or 1FK1164 with an expiration date of January 31, 2023.
Look for the NDC code 11822-6319-1 and batch numbers 1BK0964 or 1FK1164 on the product label.
The product was manufactured with a contaminated excipient that was recalled from the excipient supplier.
Check for NDC code 11822-6319-1 and batch numbers 1BK0964 or 1FK1164 with an expiration date of January 31, 2023.
The recall record does not specify a remedy, so contact Rite Aid for further instructions.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0621-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0621-2022 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.
