Home/Recalls/FDA-Z-2535-2026
FDA DevicesClass II

Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590

Published: July 8, 2026Recall ID: Z-2535-2026Category: devicesCountry: US

Reason for Recall / Hazard

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Product Description & Identification

Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590

Affected Products

Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id99162
Address 13 Lakes Dr
Address 2N/A
Code info1) DYNJRA1590, UDI-DI: 10193489284829(each), 40193489284820(case), Lot Number: 25JLA522
Postal code60093-2753
Report date20260708
Product typeDevices
Product quantity270 kits
Reason for recallThe kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260521
Initial firm notificationLetter
Center classification date20260629

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution.
Official Agency Alert