Peter Laz: D-Clip Applier Fails During Surgery - Recall

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Recalling firmPeter Lazic GmbhImmelmannweg 2, N/A · Tuttlingen, N/A N/A

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Peter Lazic recalls certain surgical appliers that can fail during procedures, leaving the clip attached to the patient. This poses a risk of injury if the clip does not release properly during surgery.

Why it’s dangerous

The applier may fail to release the clip during surgery, causing it to remain attached to the patient. This could lead to injury if the clip does not detach as intended.

Who’s affected

Surgical professionals using the D-Clip Standard/Mini Applier for procedures are most at risk. Patients undergoing surgery with this device could be affected if the clip fails to release.

How to tell if you have this one

Check for model number 35.411 on the applier. Look for UDI/DI number 04250603739609. All lot numbers are affected.

Brand
Peter Lazic
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Applier Model
Verify the model number is 35.411 on the D-Clip Standard/Mini Applier.
Contact Manufacturer
Reach out to Peter Lazic Gmbh for further assistance or to confirm if your unit is affected.

✎ GovInfoNow

Questions people ask

Is this recall for home use?

No, this recall is specific to surgical use only.

How can I tell if my applier is affected?

Check for model number 35.411 and UDI/DI number 04250603739609.

What should I do if I have this applier?

Contact Peter Lazic Gmbh to confirm if your unit is affected and for further instructions.

Take action

Contact Peter Lazic

We’ve drafted a message you can send Peter Lazic to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1278-2024 — Peter Lazic Peter Lazic

Hello,

I own a Peter Lazic that is covered by recall Z-1278-2024 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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Where this comes from

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.

Official source: FDA Recall #Z-1278-2024 (October 6, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1278-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Peter Lazic Gmbh recalls D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.

Use caution until it’s fixed