Reported Jul 21, 2021 · Terminated
Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, packaged in 80-count canister…
Sanit Technologies, LLC dba Durisan
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Sanit Technologies, LLC dba Durisan · 7810 25th Ct E Unit 106 · Sarasota, FL · 34243-2841
Is this the product you have?
- 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.
- Lot codes and dates
25 of 25 products
Products covered by this recall # Product as published 1 DHS041519A1-S, DHS041519A2-S, DHS041519A3-S, DHS041519A4-S, DHS041519A5-S, DHS041519A6-S, Exp. 5/15/2021 2 DHS042919AR1-S, Exp. 5/29/2021 3 DHS043019AR1-S, Exp. 5/30/2021 4 DHS050319A4-S, Exp. 6/03/2021 5 DHS053019A1-S, DHS053019A2-S, DHS053019A4-S, DHS053019A5-S, DHS053019A6-S, Exp. 6/30/2021 6 DHS070219A1-S, DHS070219A2-S, DHS070219A3-S, DHS070219A4-S, DHS070219A5-S, DHS070219A6-S, DHS070219AB-S, Exp. 8/2/2021 7 DHS080219A1-S, Exp. 9/2/2021 8 DHS091819A1-S, Exp 10/18/2021 9 DHS032820B1-S, Exp 4/28/2022 10 DHS051520A1R1-S, Exp. 6/15/2022 11 DHS052020A1R1-S, DHS052020B1R1-S, DHS052020CR1-S, Exp. 6/20/2022 12 DHS052220A1R1-S, Exp. 6/22/2022 13 DHS052720C1R1-S, Exp 6/27/2022 14 DHS052920A1R1-S, DHS052920B1R1-S, DHS052920C1R1-S, Exp 6/29/2022 15 DHS060320C1R1-S, Exp. 7/3/2022 16 DHS060520C1R1-S, DHS060520F1R1-S, Exp. 7/5/2022 17 DHS060820E1R1-S, Exp. 7/8/2022 18 DHS061220A1R1-S, Exp. 7/12/2022 19 DHS061920B1R1-S, Exp. 7/19/2022 20 DHS062320B1R1-S, Exp. 7/23/2022 - Amount recalled
- 43,164 canisters TOTAL
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.
This product could cause temporary or reversible health problems — stop using it.
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