Seatex LLC 2024-03-06 Health serious FDA
Health · FDA · Recall #FDA-D-0357-2024
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex… Recall
Issued March 6, 2024 · Seatex LLC
In March 2024, Seatex LLC recalled the PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
What you should do
- 1 Stop using PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Seatex LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Seatex LLC
- Category
- Health
- Recall date
- March 6, 2024
- Units affected
- Not reported
- Sold at
- Nationwide in the US and Puerto Rico
- Recall number
- FDA-D-0357-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Seatex LLC has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.