FDA Media Alert Detail

Device Recall

FDA Device Recall: Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

  • U.S. Food and Drug Administration
  • September 2, 2026
  • ID: device-Z-3006-2026

Device Enforcement Report Details

Recall NumberZ-3006-2026
Recalling FirmAVID Medical, Inc.
ClassificationClass II
Voluntary / MandatedVoluntary: Firm initiated
Distribution PatternUS Nationwide distribution in the states of MS, TX.
StatusOngoing
Device ClassN/A
Device NameN/A
Product Description

Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03

Reason for Recall

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Code Information

Lot Code: Lot Number: 1632948 UDI: 10809160423578


Content syndicated from the U.S. Food and Drug Administration (FDA) device enforcement reports database.