Home/Recalls/FDA-Z-1404-2026
FDA DevicesClass II

Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PAC...

Published: February 25, 2026Recall ID: Z-1404-2026Category: devicesCountry: US

Reason for Recall / Hazard

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

Product Description & Identification

Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PACK-LF, Model Number: DYNJ42829B; 3) BURN CARE PACK-LF, Model Number: DYNJT3437

Affected Products

Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PACK-LF, Model Number: DYNJ42829B; 3) BURN CARE PACK-LF, Model Number: DYNJT3437

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98329
Address 13 Lakes Dr
Code info1) DYNJ15668R, UDI-DI: 10195327108502(each), 40195327108503(case), Lot Number: 23HMB037; 2) DYNJ42829B, UDI-DI: 10193489880151(each), 40193489880152(case), Lot Number: 22IBI084; 3) DYNJT3437, UDI-DI: 10198459325076(each), 40198459325077(case), Lot Number: 25FBK633
Postal code60093-2753
Report date20260225
Product typeDevices
Product quantity291 units
Reason for recallMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260107
Initial firm notificationLetter
Center classification date20260217

Overview

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