TemporaryFDAOngoing
Can cause harm that is usually temporary.
DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
Check the device or its packaging for
1. Model/Item Number (Kit): SAMM064-27; UDI-DI: 10809160439708; Kit Lot Numbers: 1657586, 1658104, 1671251; 2. Model/Item Number (Kit): SAMM064-28; UDI-DI: 10809160516201; Kit Lot Numbers: 1698700; Recalled Supplier Component (in kit): A303416A; Recalled Supplier Lot Number (in kit): NGKU1749, NGKV0359;
- Why
- Product may be potentially contaminated with a lubricant used during the manufacturing process.
- Distributed
- US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
- Company
- AVID Medical, Inc.
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-0092-2027 · retrieved 7 October 2026
Read the official notice