Water-jel Technologies, Llc: Lidocaine Wound Gel (benzalkonium Chloride, 0.13% And Lidocaine Hydrochloride, 2%)
Recall Summary CVS Pharmacy's Lidocaine Wound Gel (0.5 oz tubes, NDC 59898-950) is being recalled nationwide because the product failed to meet required pH specifications. The gel, which contains lidocaine and benzalkonium chloride for wound care, was distributed across all U.S. states and Washington, D.C. This is classified as a Class III recall, the least severe classification.
- Recalling firm
- Water-Jel Technologies, LLC
- Product
- Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
- Reason
- Failed PH Specifications
- Classification
- Class III
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-04-07
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide in the USA
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/8f241cdc-a292-4761-9140-a26e48896ad9