# FDA recall Z-2450-2024

> **Zimmer, Inc.** · Class II · device recall initiated 2024-07-02.

## Product

CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis, used in Hip Arthroplasty; Item Numbers 00811400000  00811400010  00811400100  00811400110  00811400200  00811400210  00811400218  00811400230  00811400300  00811400310  00811400318  00811400330  00811400400  00811400410  00811400420  00811400423  00811400426  00811400430  00811400500  00811400510  00811400530  00811401218  00811401318  00811404000  00811405000

## Reason for recall

Affected product has an increased risk of postoperative perisprosthetic femoral fracture (PFF). The IFU is being updated to reflect the risk of PFF.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2450-2024
- **Recalling firm:** Zimmer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-02
- **Report date:** 2024-08-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2450-2024

## Citation

> AI Analytics. FDA recall Z-2450-2024. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-2450-2024. Source: US FDA. Licensed CC0.

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