# FDA recall Z-1087-2019

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-03-01.

## Product

Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile Titanium, Accessory to total hip implant  Item Number: 103533    Product Usage:  Accessory to total hip implant

## Reason for recall

Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have the potential for the 30mm screws to be packaged as 20mm screws and vice versa.

## Distribution

Worldwide Distribution - US Nationwide  Foreign:  CHILE           CHINA                COSTA RICA                 GUJRAT,INDIA      JAPAN            MEXICO CDMX       SINGAPORE

## Key facts

- **Recall number:** Z-1087-2019
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-01
- **Report date:** 2019-04-10
- **Termination date:** 2020-05-27

- **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-1087-2019

## Citation

> AI Analytics. FDA recall Z-1087-2019. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-1087-2019. Source: US FDA. Licensed CC0.

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