D-Clip Applier (Peter Lazic) – Surgery Failure Risk (2023)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Brand
Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany
Lot Codes / Batch Numbers
Model number: 35.410, UDI/DI: 04250603739593, All Lot numbers.
Products Sold
Model number: 35.410; UDI/DI: 04250603739593; All Lot numbers.
Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany is recalling D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action. due to Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to th. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Recommended Action
Per FDA guidance
Reportable Event - Removal letters dated October 6, 2023 were sent to customers. Customers were instructed to return all product subject to recall and to notify any of their customers as well. Please return items for the attention of one of the PRRCs provided to ensure quick processing and assignment to the case. If you have any questions, please contact Mr. Sven Lazic (info@lazic.de +49 (0) 7461 96643 - 20) or Ms. Kim Maier (k.maier@lazic.de or +49 (0) 7461 96643 - 21).
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