# FDA recall Z-0074-2024

> **Flower Orthopedics Corporation** · Class II · device recall initiated 2023-08-29.

## Product

Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the intramedullary canal to the appropriate depth for nail insertion; Flex-Thread TM 3.2mm is provided sterile, single use.    Catalogue Number: 8528-1-S

## Reason for recall

Device is breaking while in use, potential for patients to require a revision surgery.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0074-2024
- **Recalling firm:** Flower Orthopedics Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-29
- **Report date:** 2023-10-18

- **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-0074-2024

## Citation

> AI Analytics. FDA recall Z-0074-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0074-2024. Source: US FDA. Licensed CC0.

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