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
- Recalling Firm
- Sanit Technologies, LLC dba Durisan
- 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.
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