Home/Recalls/FDA-Z-2235-2026
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Published: June 3, 2026Recall ID: Z-2235-2026Category: devicesCountry: US

Reason for Recall / Hazard

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.

Product Description & Identification

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026

Affected Products

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98837
Address 13 Lakes Dr
Code infoMedline Kit SKU DYNJRA9026: UDI/DI 10884389285688 each, 40884389285689, case, Lot Numbers: 26BBD235, 26ABB534, 25DBT837, 25CBH118, 24FBT403, 24FBJ505.
Postal code60093-2753
Report date20260603
Product typeDevices
Product quantity4370 kits
Reason for recallMedline 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260410
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260528

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass I
  • DistributionWorldwide - US Nationwide distribution in the US Territory of Virgin Islands and the countries of Bahamas, Panama, Barbados.
Official Agency Alert