Official recall notice

FDA DeviceClass IINotable

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

Recall date
2026-09-02
FDA class
Class II

Why it was recalled

Hazard

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

Product description

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

Affected products

Lot Code: Lot Number: 1649519 UDI: 10809160457887

Verify with the official notice →
Share:

Related Recalls

2026-09-16 · FDA_DEVICE
FDA Recall: Halyard IV Start Kit Non-Sterile REF: KRIV26-02
AVID Medical, Inc.
2026-09-09 · FDA_DEVICE
FDA Recall: Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22
AVID Medical, Inc.
2026-09-09 · FDA_DEVICE
FDA Recall: Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT,
AVID Medical, Inc.
2026-09-09 · FDA_DEVICE
FDA Recall: 1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPIN
AVID Medical, Inc.