The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-0926-2026·Announced 2025-12-24

Laparoscopy packs recalled over a potentially incomplete header bag seal

AVID Medical is recalling 42 Halyard General Laparoscopy Packs over the potential for an incomplete seal on the header bag.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Scored 3 under the risk-of-harm criterion: an incomplete package seal affects the sterile barrier of a procedure pack, and no injuries are reported.

Plain-English summary

The Halyard GENERAL LAPAROSCOPY PACK, catalog number VAST018-10, is being recalled by AVID Medical, Inc.

The reason given in the enforcement record is the potential for an incomplete seal on the header bag.

The record lists 42 units carrying UDI-DI 10809160452257, from lot 1651776 with an expiration of 3/12/2027. Distribution was in Georgia, Illinois, Nebraska and Maryland. The FDA has classified the action as Class II.

An incomplete seal on the packaging affects the sterile barrier of a procedure pack. The enforcement record reports no injuries. Facilities should quarantine the affected lot and follow the firm's instructions.

The recalled product

Product
Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.
Manufacturer
AVID Medical, Inc.
Affected units
42

Distribution

Distributed in 4 states:

Part of a larger recall action

This product is one of 5 recalled by AVID Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 5 products in this recall →

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