Seatex recalls PROBLEND Antibacterial Foaming Silk Hand Sanitizer due to FDA inspection finding manufacturing deficiencies. Products with specific lot numbers and expiration dates are affected.
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Seatex is recalling PROBLEND Antibacterial Foaming Silk Hand Sanitizer products because an FDA inspection found manufacturing deficiencies at their facility. This recall affects specific lot numbers and expiration dates of the sanitizer.
The FDA identified manufacturing deficiencies during an inspection of Seatex's facility. These deficiencies could potentially impact product safety and quality, but the specific risks are not detailed in the recall notice.
Owners of PROBLEND Antibacterial Foaming Silk Hand Sanitizer products with the listed lot numbers and expiration dates are affected. People using these products for hand hygiene are most at risk.
Check the product label for lot numbers: 263647 (exp. 06/09/2024), 271382 (exp. 01/18/2025), 261675 (exp. 04/09/2024), or 272766 (exp. 02/15/2025). The product comes in 1250 mL or 1 G cases with mountain spring scent.
Look for lot numbers: 263647 (exp. 06/09/2024), 271382 (exp. 01/18/2025), 261675 (exp. 04/09/2024), or 272766 (exp. 02/15/2025).
The FDA identified manufacturing deficiencies during an inspection of Seatex's facility.
Check the product label for the listed lot numbers and expiration dates. If you have one, contact Seatex for instructions.
The recall notice does not specify the risk of injury, only that manufacturing deficiencies were found during an FDA inspection.
We’ve drafted a message you can send Seatex to request your refund or repair — edit it as you like.
Subject: Recall D-0356-2024 — Seatex Seatex Hello, I own a Seatex that is covered by recall D-0356-2024 from Seatex. 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.
