PlainRecalls
FDA Drug Moderate Class II Terminated

Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, packaged in 80-count canister (UPC 8 52379 00632 5), b) 160-count canister (UPC 8 52379 00631 8), and c) 240-count canister (UPC 8 52379 00633 2); Sanit Technologies, LLC, 7810 25th Court East, Sarasota, Florida 34243.

Reported: July 21, 2021 Initiated: March 10, 2021 #D-0659-2021

Product Description

Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, packaged in 80-count canister (UPC 8 52379 00632 5), b) 160-count canister (UPC 8 52379 00631 8), and c) 240-count canister (UPC 8 52379 00633 2); Sanit Technologies, LLC, 7810 25th Court East, Sarasota, Florida 34243.

Reason for Recall

CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.

Details

Units Affected
43,164 canisters TOTAL
Distribution
Nationwide in the USA and Bahamas
Location
Sarasota, FL

Frequently Asked Questions

What product was recalled?
Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, packaged in 80-count canister (UPC 8 52379 00632 5), b) 160-count canister (UPC 8 52379 00631 8), and c) 240-count canister (UPC 8 52379 00633 2); Sanit Technologies, LLC, 7810 25th Court East, Sarasota, Florida 34243.. Recalled by Sanit Technologies, LLC dba Durisan. Units affected: 43,164 canisters TOTAL.
Why was this product recalled?
CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 21, 2021. Severity: Moderate. Recall number: D-0659-2021.