Perrigo recalls Severe Congestion Nasal Spray with contaminated ingredients. Products distributed by Rite Aid may cause health risks. Consumers should check NDC 11822-6378-1 and batch 11BK0827 for affected items.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling Severe Congestion Nasal Spray due to contaminated ingredients that could pose health risks. This recall affects products distributed by Rite Aid with specific NDC and batch numbers. Using these products may lead to potential health issues from the contaminated excipient.
The nasal spray was manufactured using a contaminated excipient that was previously recalled by the supplier. This contamination could lead to health risks when the product is used, though the exact nature of the risk is not specified in the recall notice.
People who own or use the Severe Congestion Nasal Spray with NDC 11822-6378-1 and batch 11BK0827 are affected. Those with respiratory conditions may be at higher risk due to potential contamination.
Check for the NDC code 11822-6378-1 and batch number 11BK0827 on the product label. The product was distributed by Rite Aid in the United States.
Look for NDC 11822-6378-1 and batch 11BK0827 on the label to confirm if the product is affected.
The recall states the product was manufactured with a contaminated excipient, but the exact health risk is not specified. Consumers should check if they have the affected batch and NDC number.
Check the product label for NDC 11822-6378-1 and batch number 11BK0827. The product was distributed by Rite Aid.
The recall does not specify a remedy, so consumers should check with the manufacturer or contact Rite Aid 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-0608-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0608-2022 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.
