# FDA recall Z-1698-2021

> **Flower Orthopedics Corporation** · Class II · device recall initiated 2021-04-15.

## Product

T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm    Product Code: GWK 300

## Reason for recall

Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages

## Distribution

US Nationwide distribution in the states of AZ, CO, FL, GA, IL, IN, PA, NC, VA.

## Key facts

- **Recall number:** Z-1698-2021
- **Recalling firm:** Flower Orthopedics Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-04-15
- **Report date:** 2021-06-09
- **Termination date:** 2021-11-12

- **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-1698-2021

## Citation

> AI Analytics. FDA recall Z-1698-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1698-2021. Source: US FDA. Licensed CC0.

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