Perrigo recalls nasal spray decongestant due to contaminated excipient from supplier. Products distributed by Kroger may pose health risks. Consumers should check NDC 30142-388-10 and batch 1BK0826.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling nasal spray decongestants that were made with a contaminated ingredient. This could lead to health issues if the product is used. Affected products have specific NDC and batch numbers.
The product was manufactured using an excipient (a substance added to the product) that was contaminated. This contamination could cause health issues if the product is used. The specific contaminant was recalled by the excipient supplier.
People who own or use the recalled nasal spray decongestant with NDC 30142-388-10 and batch 1BK0826 are affected. Those with allergies to the ingredients or who use the product frequently may be at higher risk.
Check for the NDC code 30142-388-10 and batch number 1BK0826 on the product label. The product was distributed by Kroger in the United States.
Look for the NDC code 30142-388-10 and batch number 1BK0826 on the product label.
The product was manufactured with a contaminated excipient, which could pose health risks. It is recommended to stop using the product if you have the recalled batch.
Check the product label for the NDC code 30142-388-10 and batch number 1BK0826. If you have the recalled product, you should stop using it.
Look for the NDC code 30142-388-10 and batch number 1BK0826 on the product label. The product was distributed by Kroger in the United States.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0617-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0617-2022 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.
