Fresh Recalls

FDAClass II · Medical device · Recall Z-2410-2026 · Recalled June 17, 2026

Halyard recall — AVID Medical, Inc.

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Halyard
Company / brand
AVID Medical
Lot / serial / date codes
Kit Code: UIEB48-01. UDI-DI: 10809160484098. Lot Number: UIEB48-01. Expiration Date: 8/7/2028.
Distribution
US Nationwide distribution in the state of Iowa.
Agency product description and boundaries

Halyard, Eye Bag Pack. Kit Code: UIEB48-01.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Halyard

3. Open the official notice or contact

Official recall ID
Z-2410-2026
Brand
AVID Medical
Classification
Class II
Units affected
60 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Toano, VA, United States
Firm address
9000 Westmont Dr, N/A, 23168-9351

Identifying details (verbatim from the notice)

Product codes / lots
Kit Code: UIEB48-01. UDI-DI: 10809160484098. Lot Number: UIEB48-01. Expiration Date: 8/7/2028.
Distribution
US Nationwide distribution in the state of Iowa.
Firm notified the public via
E-Mail
FDA event ID
99021
Recall initiated
April 30, 2026
FDA classified
June 11, 2026
FDA report date
June 17, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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