Reported Nov 20, 2024 · Ongoing
Halyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-02
AVID Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: AVID Medical, Inc. · 9000 Westmont Dr · Toano, VA · 23168-9351
Is this the product you have?
- Halyard KIT, SPINE -
- Medical convenience kits Model NumberEUOR004-02
- Lot codes and dates
- GTIN10809160366479
- Lot Number1600550
- Amount recalled
- 165 eaches
This recall covers 73 products
The agency filed one notice per product. You are reading one of them; the other 72 are below.
60 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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