PROBLEND Antibacterial Foaming Silk All-In-One Foaming recall: CGMP Deviations
PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G…
Why was PROBLEND Antibacterial Foaming Silk All-In-One Foaming 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 #s: a) 263647, Exp. 06/09/2024; 271382, Exp. 01/18/2025; b) 261675, Exp. 04/09/2024; 263647, Exp. 06/09/2024; 272766, Exp.02/15/2025.
- Product
- PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G…
- Recalling firm
- Seatex LLC
- Quantity
- 1,450 cases
- Distribution
- Nationwide in the US and Puerto Rico
- Recall date
- March 6, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)