Recall
ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
AVID Medical, Inc. · 10 Aug 2026
- Status
- Recall open, classified
- Why, in the FDA's words
- “Product may be potentially contaminated with a lubricant used during the manufacturing process.”
- Recall began
- 10 Aug 2026
- Company
- AVID Medical, Inc.
- Device type
- Product code (OEZ)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.