Reported Oct 14, 2026 · Ongoing
ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
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?
- ENDOVASCULAR PACK
- Model/Item Number (Kit)VAPX014-04
- Lot codes and dates
- 1
- Model/Item Number (Kit)VAPX014-04
- UDI-DI10809160332863
- Kit Lot Numbers
170110617021751702273
- Recalled Supplier Component (in kit)A902416
- Recalled Supplier Lot Number (in kit)NGKU4043
- Amount recalled
- 33
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Product may be potentially contaminated with a lubricant used during the manufacturing process.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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