Recall Z-0098-2027— AVID Medical, Inc.
Class II · Ongoing
Class II FDA medical device recall by AVID Medical, Inc., initiated 2026-08-10. FDA's recall record names no specific 510(k) clearance for this event. Product: ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;. Reason: Product may be potentially contaminated with a lubricant used during the manufacturing process..
- Recalling firm
- AVID Medical, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-08-10
- Firm location
- Toano, VA, United States
Product description
ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
Reason for recall
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Data sourced from openFDA. This site is unofficial and independent of the FDA.