FDAFDA recall Z-0095-2027 · Oct 14, 2026
AVID Medical, Inc.: ENDOVASCULAR PACK recall
Recall found
Product
ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
Reason for recall
Product may be potentially contaminated with a lubricant used during the manufacturing process.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- 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;
- Quantity
- 33
- Distribution
- US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
- Recalling firm
- AVID Medical, Inc., Toano, VA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-10
Source: openFDA enforcement record Z-0095-2027 · search recall number Z-0095-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.