AVID Medical, Inc.: Medical Device Recall in 2024 - (Recall #: Z-0414-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Halyard ANGIO ARTERIOGRAM PACK - Medical convenience kits Model Number: MMCC004-01

Product Classification:

Class II

Date Initiated: September 20, 2024

Date Posted: November 20, 2024

Recall Number: Z-0414-2025

Event ID: 95515

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

Status: Ongoing

Product Quantity: 176 eaches

Code Information:

GTIN: 10809160421772 Lot Number: 1605588, 1605589

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated