# FDA recall Z-1302-2019

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-03-28.

## Product

T7 Driver Cannulated AO (Part Number 110018531)    Product Usage:  The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and phalanges of the foot or the phalanges, metacarpals and carpals of the hand. In the foot, these include procedures to correct Hallux Valgus (bunions), Hallux Varus and Hallux Rigidus, Hammer toe, Claw toe and Mallet toe.

## Reason for recall

There is a potential of fracture, bending or shearing of the driver.

## Distribution

Worldwide Distribution - US Nationwide in the states:  AK, AL, AR, AZ,  CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NJ, NM, NY, OH, OK, OR, PA, RI, SC< SD< TN, TX, UT, VA, VT, WA, WI, and WY.    The products were distributed to the following foreign countries:  Australia, Canada, Costa Rica, Malaysia, Netherlands, and Singapore.

## Key facts

- **Recall number:** Z-1302-2019
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-28
- **Report date:** 2019-05-15
- **Termination date:** 2020-06-02

- **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-1302-2019

## Citation

> AI Analytics. FDA recall Z-1302-2019. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1302-2019. Source: US FDA. Licensed CC0.

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