Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream Recalled by Flower Orthopedics Corporation Due to Device is breaking while in use, potential for...

Date: August 29, 2023
Company: Flower Orthopedics Corporation
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Flower Orthopedics Corporation directly.

Affected Products

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

Quantity: 70 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Flower Orthopedics Corporation

Flower Orthopedics Corporation has 16 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report