FDA Medical devices recall ·
DAVINCI LAP/GYN recall
- Recall number
- Z-0101-2027
- Date
- (initiated August 10, 2026)
- Company / brand
- AVID Medical, Inc.
9000 Westmont Dr, Toano, VA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 30
- Hazard tags
- Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
Why was it recalled?
Product may be potentially contaminated with a lubricant used during the manufacturing process.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model/Item Number (Kit): WRNM037-16; UDI-DI: 10809160468913; Kit Lot Numbers: 1663589; Recalled Supplier Component (in kit): A942216; Recalled Supplier Lot Number (in kit): NGKT3375;
Distribution
US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
States: Arizona California Florida Maryland Nebraska Texas
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0101-2027. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.