Perrigo recalls nasal decongestant spray due to contaminated ingredients from supplier. Products may pose health risks; check NDC codes and batch numbers for affected items.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling nasal decongestant spray bottles that were made with contaminated ingredients. Using these products could expose you to harmful substances from the supplier's recalled excipient.
The spray was manufactured using an excipient (ingredient) that was recalled by the supplier due to contamination. This could lead to health risks if the contaminated ingredient is absorbed through the nasal passages.
People who own or use the recalled nasal decongestant spray bottles. Those with sensitive health conditions may be at higher risk due to potential contamination.
Check for NDC code 0904-6761-30 and batch numbers 1BK0826 (expiring 12/31/2022) or 1FK1164 (expiring 01/31/2023). The product is sold by Major Pharmaceuticals in Livonia, Michigan.
Look for NDC code 0904-6761-30 and batch numbers 1BK0826 or 1FK1164 on the bottle.
The recall states the product was made with contaminated ingredients, so it is not safe to use. The manufacturer recommends checking if you have the affected batch numbers.
Check the NDC code and batch numbers on the bottle. If it matches the recalled items, stop using it and contact the manufacturer for further instructions.
Look for NDC code 0904-6761-30 and batch numbers 1BK0826 (expiring 12/31/2022) or 1FK1164 (expiring 01/31/2023) on the bottle label.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0618-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0618-2022 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.
