# FDA recall Z-2428-2020

> **PROVIDENCE MEDICAL TECHNOLOGIES** · Class II · device recall initiated 2019-03-29.

## Product

Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. L Providence Medical Technology, Inc. 3875 Hopyard Road, Suite 300, Pleasanton, CA  94588, Rx Only.

## Reason for recall

There may be dimensional manufacturing error that represents a potential safety risk to patients.

## Distribution

US Nationwide distribution including in the states of AZ, CA, FL, IL, IN, LA, MA, MO, NC, NJ, NY, OH, OR and TX.

## Key facts

- **Recall number:** Z-2428-2020
- **Recalling firm:** PROVIDENCE MEDICAL TECHNOLOGIES
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-29
- **Report date:** 2020-07-01
- **Termination date:** 2022-05-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Pleasanton, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2428-2020

## Citation

> AI Analytics. FDA recall Z-2428-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2428-2020. Source: US FDA. Licensed CC0.

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