Nerve Block Tray

Recall Summary Medline is recalling two nerve block trays (SKUs DYNJRA1181C and DYNJRA1860) that contain a numbing medication made by Huons Co. because the medication was found to have quality issues, including problems with testing data and reports that it wasn't working as intended. The affected kits were distributed nationwide in the US, as well as in the US Virgin Islands, Bahamas, Panama, and Barbados.

Product
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.
Reason
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-04-10
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Worldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a4d6ce2f-6ade-4b1d-8cc5-d3e8c6e83bb6