Perrigo Company recalls Maximum Strength No Drip Nasal Spray with contaminated excipient. Products distributed by Kroger, NDC 30142-388-10, batch 1BK0826, exp 12/31/2022. Consumers should check labels and contact retailer.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling Maximum Strength No Drip Nasal Spray because it was made with a contaminated ingredient. This could pose a health risk if the product is used. Affected products have a specific batch number and expiration date.
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, but the risk is not severe enough to cause serious injury in normal use.
People who own or use the recalled nasal spray, especially those who have the specific batch number 1BK0826 and expiration date 12/31/2022. Those with allergies to the ingredients may be at higher risk.
Check the product label for the batch number 1BK0826 and expiration date 12/31/2022. The product is distributed by Kroger and has NDC code 30142-388-10.
Look for the batch number 1BK0826 and expiration date 12/31/2022 on the product label.
The product was made with a contaminated ingredient, so it is not safe to use. However, the risk is low and does not typically cause serious injury.
Check the product label for the batch number 1BK0826 and expiration date 12/31/2022. The product is distributed by Kroger and has NDC code 30142-388-10.
The recall record does not specify a remedy, so contact the manufacturer or retailer 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-0624-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0624-2022 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.
