Fresh Recalls

FDAClass I · Medical device · Recall Z-2796-2026 · Recalled August 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.

Agency report date: August 12, 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 convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma
Company / brand
AVID Medical
Lot / serial / date codes
UDI-DI 10809160377314 Lots 1573593 1583827 1609541 1612134 1612516 1619132 1623384 1627013 1635459 1672306 1675159
Distribution
US Nationwide distribution in the states of NC and TX.
Agency product description and boundaries

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05

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: Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.

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

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma

3. Open the official notice or contact

Official recall ID
Z-2796-2026
Brand
AVID Medical
Classification
Class I
Units affected
5168 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

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

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI 10809160377314 Lots 1573593 1583827 1609541 1612134 1612516 1619132 1623384 1627013 1635459 1672306 1675159
Distribution
US Nationwide distribution in the states of NC and TX.
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99339
Recall initiated
April 30, 2026
FDA classified
July 31, 2026
FDA report date
August 12, 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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