AVID Medical, Inc.: ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
Read the official notice at FDA (device) →
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- AVID Medical, Inc.
- Product
- ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
- Reason / hazard
- Product may be potentially contaminated with a lubricant used during the manufacturing process.
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
- Recall initiated
- 2026-08-10
- Code info
- 1. Model/Item Number (Kit): VAPX014-04; UDI-DI: 10809160332863; Kit Lot Numbers: 1701106, 1702175, 1702273; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU4043;
- Product quantity
- 33
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Toano
- State
- VA
- Country
- United States
- Event id
- 99808
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