Z-0415-2025 Class II Ongoing

Recalled by AVID Medical, Inc. — Toano, VA

FDA device recall Z-0415-2025 was initiated by AVID Medical, Inc. on September 20, 2024 and is designated Class II. Reason for recall: Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing… The recall status is ongoing. Affected quantity: 44 eaches.

Recall Details

Product Type
Devices
Report Date
November 20, 2024
Initiation Date
September 20, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
44 eaches

Product Description

Halyard ORTHO PACK -Medical convenience kits Model Number: MMOK006-04

Reason for Recall

Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions

Distribution Pattern

US Nationwide distribution.

Code Information

GTIN: 10809160404201 Lot Number: 1597105,1605626