D-Clip Standard/Mini Applier recall
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
Why was D-Clip Standard/Mini Applier recalled?
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model number: 35.411; UDI/DI: 04250603739609; All Lot numbers.
- Product
- D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
- Recalling firm
- Peter Lazic Gmbh
- Quantity
- 63 units
- Distribution
- US Nationwide distribution in the state of ME.
- Recall date
- March 20, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)