Medtronic Cardiac Surgery Technologies Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip Anastomotic Device Removal Tool is designed to remove U-Clip Anastomotic Devices. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip Anastomotic Device Removal Tool is designed to remove U-Clip Anastomotic Devices.
Brand
Medtronic Cardiac Surgery Technologies
Lot Codes / Batch Numbers
lot numbers: 0610707, 0614409, 0614410, 0614411, 0614412, 0622204
Products Sold
lot numbers: 0610707, 0614409, 0614410, 0614411, 0614412, 0622204
Medtronic Cardiac Surgery Technologies is recalling Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip Anastomotic Device Re due to Six lots of U-Clip Removal Tools, catalog REM1860FW were incorrectly assembled. The nose cone attachment to the body of the removal tool does not con. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Six lots of U-Clip Removal Tools, catalog REM1860FW were incorrectly assembled. The nose cone attachment to the body of the removal tool does not contain sufficient adhesive which can cause the nose to separate from the body of the device.
Recommended Action
Per FDA guidance
Customers to be notified via a letter on 2/8/07. The letter will explain the situation and requests that the impacted product be returned to Medtronic for disposal. The customer will be requested to complete a "Recall Certificate" acknowledging the receipt of this information.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026