Perrigo Company PLC recalls Maxiumum Strength No Drip Nasal Spray with contaminated excipient. Products distributed by Old East Main Co. in Tennessee. Consumers should check NDC numbers and batch dates 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. This could pose a health risk if the contaminated material enters the body through nasal use.
The nasal spray was manufactured using an excipient (ingredient) that was recalled by the supplier due to contamination. This contamination could potentially enter the body through nasal use, though the specific health risk is not detailed in the recall.
People who own or use the recalled Maxiumum Strength No Drip Nasal Spray. Those with sensitive health conditions may be at slightly higher risk due to potential contamination.
Check for NDC number 55910-623-10 with batch 1BK0826 (expiring 12/31/2022) or batch 1FK1232, 1BK0964 (expiring 01/31/2023). Products were distributed by Old East Main Co. in Goodletttsville, Tennessee.
Look for NDC number 55910-623-10 with batch numbers 1BK0826 (expiring 12/31/2022) or 1FK1232, 1BK0964 (expiring 01/31/2023).
The recall states the product was manufactured with a contaminated excipient, but the specific health risk is not detailed. Consumers should check if they have the recalled batch numbers.
Check for NDC number 55910-623-10 with batch numbers 1BK0826 (expiring 12/31/2022) or 1FK1232, 1BK0964 (expiring 01/31/2023).
The recall does not specify a remedy, so consumers should check with the manufacturer or contact the distributor 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-0616-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0616-2022 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.
