Home/Recalls/FDA-Z-1000-2026
FDA DevicesClass I

Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.

Published: January 14, 2026Recall ID: Z-1000-2026Category: devicesCountry: US

Reason for Recall / Hazard

Devices are not suitable for organ transplant.

Product Description & Identification

Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.

Additional Source Details

FieldValue
CityToano
StateVA
Event id98060
Address 19000 Westmont Dr
Code infoKit Code: LLOG1000-15; UDI: 10809160432679; Lot No: 1632138 & 1648393.
Postal code23168-9351
Report date20260114
Product typeDevices
Product quantity132 units
Reason for recallDevices are not suitable for organ transplant.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251111
Initial firm notificationE-Mail
Center classification date20260102

Overview

  • Recalling FirmAVID Medical, Inc.
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS Nationwide distribution in the states of FL, GA and Puerto Rico.
Official Agency Alert