The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-2410-2026·Announced 2026-06-17

Halyard eye bag packs shipped without validated sterilization in Iowa

Halyard Eye Bag Packs, kit code UIEB48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 60 kits affected.

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: FDA Class II recall where surgical kits were distributed without validated sterilization, a risk of harm with no injuries reported in the source.

Plain-English summary

The Halyard Eye Bag Pack, kit code UIEB48-01, UDI-DI 10809160484098, is being recalled. The action covers 60 kits, with an expiration date of 8/7/2028.

The stated reason is the inadvertent distribution of sealed pouches that had not undergone validated sterilization. The FDA classified the action as Class II.

Distribution was within the United States, in Iowa. The kits are supplied to healthcare facilities rather than sold to consumers.

Facilities should identify affected kits using the kit code, UDI-DI and expiration date above, quarantine them, and follow the instructions issued by the manufacturer.

The recalled product

Product
Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
Manufacturer
AVID Medical, Inc.
Affected units
60

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 4 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 4 products in this recall →

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