Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN: M006175263110
Recall
- Recall Number
- Z-1734-2020
- Event Number
- 85227
- Firm
- Boston Scientific
- FEI Number
- 3005099803
- Product Code
- EZB
- Status
- Open, Classified
- Root Cause
- Component change control
- Initiated
- March 9, 2020
- Posted
- April 1, 2020
- Address
- 100 Boston Scientific Way, Marlborough, MA, 01752-1234
Description
Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN: M006175263110
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device
Boston Scientific issued Customer Notification on March 9, 2020 stating reason for recall, health risk and action to take: cease distribution or use of any remaining product affected by this removal should cease immediately; Verify by product lot/batch number in the product table whether any product within your inventory is affected. If so, indicate on your Verification Form the quantity of units from each lot/batch that you will bereturning. As some of these products within these lots/batches are sold as 5-packs, it is important that all reported quantities represent the actual number of single units being returned and not the number of cartons/boxes or multi-packs; If you identify any product from the affected lots/batches within your inventory, please segregate the product immediately and return it to BSC in accordance with the enclosed instructions. If you are a distributor, please note that the depth is to the hospital level and this notification should be forwarded to your customers. If you are a facility that has sent products to another hospital within your network, please ensure that this notification is forwarded to them.
Nationwide Foreign: Europe, Middle East and Africa, the Americas (North America and South America, Asia Pacific and Japan
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