# FDA recall Z-0112-2022

> **Flower Orthopedics Corporation** · Class II · device recall initiated 2021-09-01.

## Product

Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with any plate as part of the Flower Small and Medium Implant Set  and uses the small locking mechanism.  Catalog Number: DBK 024

## Reason for recall

Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

## Distribution

Arizona  California  Colorado  Florida  Florida  Illinois  Indiana  Nevada  Ohio  Texas  Virginia

## Key facts

- **Recall number:** Z-0112-2022
- **Recalling firm:** Flower Orthopedics Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-09-01
- **Report date:** 2021-10-20
- **Termination date:** 2023-02-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Horsham, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0112-2022

## Citation

> AI Analytics. FDA recall Z-0112-2022. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-0112-2022. Source: US FDA. Licensed CC0.

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