# FDA recall Z-1279-2024

> **Peter Lazic Gmbh** · Class II · device recall initiated 2023-10-06.

## Product

D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.

## Reason for recall

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

## Distribution

US Nationwide distribution in the state of ME.

## Key facts

- **Recall number:** Z-1279-2024
- **Recalling firm:** Peter Lazic Gmbh
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-06
- **Report date:** 2024-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tuttlingen, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1279-2024

## Citation

> AI Analytics. FDA recall Z-1279-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1279-2024. Source: US FDA. Licensed CC0.

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