AVID Medical, Inc.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
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;
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →