# FDA recall Z-2732-2024

> **Howmedica Osteonics Corp.** · Class II · device recall initiated 2024-08-05.

## Product

Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;

## Reason for recall

A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal.

## Distribution

International distribution to the country of Australia.

## Key facts

- **Recall number:** Z-2732-2024
- **Recalling firm:** Howmedica Osteonics Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-05
- **Report date:** 2024-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2732-2024

## Citation

> AI Analytics. FDA recall Z-2732-2024. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-2732-2024. Source: US FDA. Licensed CC0.

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