# FDA recall Z-1287-2024

> **Peter Lazic Gmbh** · Class II · device recall initiated 2023-07-14.

## Product

L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile

## Reason for recall

Wrong product coloring. The paddle clips should be blank, but they are colored blue.

## Distribution

US Nationwide distribution in the state of ME.

## Key facts

- **Recall number:** Z-1287-2024
- **Recalling firm:** Peter Lazic Gmbh
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-14
- **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-1287-2024

## Citation

> AI Analytics. FDA recall Z-1287-2024. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1287-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*