Peter Lazic Gmbh recalls D-Clip Standard/Mini Appliers that may fail during surgery, causing the clip to remain attached. Affected units include model 35.410 with specific UDI/DI numbers.
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Peter Lazic recalls certain surgical clip appliers that can fail during procedures, leaving the clip attached to the tissue. This poses a risk of prolonged tissue damage during surgery if the applier doesn't release the clip.
The applier may fail to release the surgical clip during surgery, causing it to remain attached to the tissue. This can lead to prolonged tissue damage or complications if the clip doesn't detach as intended.
Surgical professionals using the D-Clip Standard/Mini Applier for procedures are most at risk. Patients undergoing surgery with this device may experience complications if the applier fails to release the clip.
Check for model number 35.410 on the D-Clip Standard/Mini Applier. The product has a UDI/DI number starting with 04250603739593. All lot numbers are affected.
Verify the model number is 35.410 on the D-Clip Standard/Mini Applier.
Reach out to Peter Lazic Gmbh for further assistance with the recall.
The recall is due to customer complaints that the applier failed during surgery, causing it to remain attached to the clip.
Check for model number 35.410 and UDI/DI number starting with 04250603739593 on the product.
Contact Peter Lazic Gmbh for guidance on next steps, as the recall remedy is not specified in the record.
We’ve drafted a message you can send Peter Lazic to request your refund or repair — edit it as you like.
Subject: Recall Z-1277-2024 — Peter Lazic Peter Lazic Hello, I own a Peter Lazic that is covered by recall Z-1277-2024 from Peter Lazic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
