Z-3009-2026 Class II Ongoing

Recalled by AVID Medical, Inc. — Toano, VA

FDA device recall Z-3009-2026 was initiated by AVID Medical, Inc. on July 9, 2026 and is designated Class II. Reason for recall: Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. The recall status is ongoing. Affected quantity: 120 Kits.

Recall Details

Product Type
Devices
Report Date
September 2, 2026
Initiation Date
July 9, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
120 Kits

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.

Distribution Pattern

US Nationwide distribution in the states of MS, TX.

Code Information

Lot Code: Lot Number: 1662335 UDI: 10809160457887