Conseal International recalls Nanosil Spray Gel due to missing lot codes and expiration dates, posing risks from unverified manufacturing practices. Consumers should check product labels for these identifiers.
A recent FDA inspection of the firm revealed significant Current Good Manufacturing Practices (cGMP) deficiencies including lack of data to support products conform to final specifications, and lack of expiration dates on the product being recalled.
Conseal International is recalling Nanosil Spray Gel (4 fl. oz.) because it lacks lot codes and expiration dates. This makes it impossible to verify the product's safety and quality, which could lead to ineffective or unsafe use.
The product does not have lot codes or expiration dates, which are required by FDA regulations to ensure product safety and quality. Without these identifiers, it's impossible to confirm the product meets current manufacturing standards or has been properly stored.
Anyone who owns or uses the Nanosil Spray Gel with missing lot codes and expiration dates. People using the product for medical purposes are most at risk due to potential ineffective treatment.
Check the product label for a lot code and expiration date. The recalled product is the Nanosil Spray Gel (4 fl. oz.) with no lot codes or expiration dates.
Look for a lot code and expiration date on the label. If missing, the product is recalled.
The product lacks lot codes and expiration dates, which are required by FDA regulations to ensure safety and quality.
Check the label for a lot code and expiration date. The recalled product does not have these identifiers.
Check the label for a lot code and expiration date. If missing, the product is recalled and should not be used.
We’ve drafted a message you can send Conseal to request your refund or repair — edit it as you like.
Subject: Recall Z-1627-2018 — Conseal Conseal Hello, I own a Conseal that is covered by recall Z-1627-2018 from Conseal. 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.
