Official recall record

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF REGIONAL SELF131-05

US FDA — Medical Devices · 2026-04-30 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2026-04-30
Country of alert: United States
Alert level: Class I
Alert type: recall
Barcode (EAN/GTIN): 10809160408650
Brand on record: AVID Medical, Inc.
Product category: Medical Device

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.

More recalls: US FDA — Medical Devices · United States · all filters

Same barcode in other registries

The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

2026-03-13 · US FDA — Medical Devices
Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.

Other recalls from this brand

All 48 official recall notices naming AVID Medical, Inc. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.