Seaway Pharma recalls Quality Choice No Drip Severe Congestion Nasal Pump Mist (NDC 63868-608-01) due to possible microbial contamination in manufacturing water. No contamination found in final products.
CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.
Seaway Pharma is recalling a nasal decongestant product due to possible microbial contamination in the manufacturing water. This recall does not pose a risk to consumers as no contamination was found in the final products.
The recall is based on possible microbial contamination in the purified water used during manufacturing. However, the company states no contamination was found in the final products, so the risk to consumers is minimal.
People who own the recalled nasal decongestant product. Those with allergies or sensitive nasal passages may be at slightly higher risk.
Check for the product name 'Quality Choice No Drip Severe Congestion Nasal Pump Mist', NDC 63868-608-01, and lot number SE23035. The product was distributed by C.D.M.A., Inc. in Novi, MI.
Look for the product name, NDC 63868-608-01, and lot number SE23035 on the bottle.
Yes, the company states no contamination was found in the final products, so it is safe to use.
The recall is due to possible microbial contamination in the manufacturing water, but no contamination was found in the final products.
Check the product details and if it matches the recall, contact Seaway Pharma for further instructions.
We’ve drafted a message you can send Seaway Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0217-2024 — Seaway Pharma Seaway Pharma Hello, I own a Seaway Pharma that is covered by recall D-0217-2024 from Seaway Pharma. 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.
