# FDA recall Z-3252-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-08-03.

## Product

Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for use in: Shoulder, Foot and Ankle, Knee, Hand and Wrist and Hip repair.Stainless Steel, Sterile Item Number: 110016992

## Reason for recall

Expiration date incorrectly listed on the label

## Distribution

AZ  CO  FL  FL  GA  LA  MA  MA  MO  NY  SC  TX

## Key facts

- **Recall number:** Z-3252-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-08-03
- **Report date:** 2018-10-03
- **Termination date:** 2020-04-10

- **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-3252-2018

## Citation

> AI Analytics. FDA recall Z-3252-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-3252-2018. Source: US FDA. Licensed CC0.

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