# FDA recall Z-1785-2024

> **Stryker Leibinger GmbH & Co. KG** · Class II · device recall initiated 2024-03-29.

## Product

Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton.  Catalog Number: 56-90614

## Reason for recall

Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-1785-2024
- **Recalling firm:** Stryker Leibinger GmbH & Co. KG
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-29
- **Report date:** 2024-05-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Freiburg Im Breisgau, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1785-2024

## Citation

> AI Analytics. FDA recall Z-1785-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1785-2024. Source: US FDA. Licensed CC0.

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