# FDA recall Z-1471-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-03-26.

## Product

Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4 mm Diameter; Item Number: 00-2228-024-00

## Reason for recall

Potential failure of sterile packaging seal.

## Distribution

US Nationwide and the following countries: Brazil, Singapore, Canada, Australia, Japan, Malaysia, Chile, Netherlands, Trinidad

## Key facts

- **Recall number:** Z-1471-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-26
- **Report date:** 2018-05-02
- **Termination date:** 2020-11-18

- **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-1471-2018

## Citation

> AI Analytics. FDA recall Z-1471-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1471-2018. Source: US FDA. Licensed CC0.

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