Perrigo recalls nasal decongestant spray due to contaminated excipient. Products may pose health risks; check NDC 41163-703-10 and batch 1BK0964 for affected items.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling nasal decongestant spray products made with a contaminated ingredient that could pose health risks. Consumers should check the product label for the specific NDC and batch number to determine if their item is affected.
The spray was manufactured using an excipient (a substance added to the product) that was contaminated. This contamination could lead to health issues, though the exact risk level is not specified in the recall notice.
People who own or use the recalled nasal decongestant spray, particularly those with sensitive health conditions or who use the product regularly. Those with compromised immune systems may be at higher risk.
Check the product label for the NDC code 41163-703-10 and batch number 1BK0964. The product was distributed by SuperValu and sold between the dates listed on the label.
Look for the NDC code 41163-703-10 and batch number 1BK0964 on the product label.
The recall notice states the product was manufactured with a contaminated excipient, but does not specify if it is safe to use. Consumers should check the label for the NDC and batch number to determine if their item is affected.
Check the product label for the NDC code 41163-703-10 and batch number 1BK0964. The product was distributed by SuperValu and sold with the expiration date of 01/31/2023.
The recall notice does not specify a remedy, so consumers should check the product label for the NDC and batch number to determine if their item is affected.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0623-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0623-2022 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.
