PROBLEND E3 Foaming Hand Sanitizer recall: CGMP Deviations
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
Why was PROBLEND E3 Foaming Hand Sanitizer recalled?
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 265029, Exp. 03/27/2024; 273759, Exp. 11/29/2024.
- Product
- PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
- Recalling firm
- Seatex LLC
- Quantity
- 274 cases
- Distribution
- Nationwide in the US and Puerto Rico
- Recall date
- March 6, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)