🔍 RecallPedia

Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.

Class I - Dangerous
🏥 Medical Devices Recalled: December 22, 2016 Flower Orthopedics Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Device Listing: D267957
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Flower Orthopedics Corporation
Reason for Recall:
The product is being recalled due to incidence and reports of the product breaking during surgery.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.

Product Codes/Lot Numbers:

Device Listing: D267957

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1113-2017

Related Recalls

Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to facilitate the insertion of the Flex-Thread Nail System- Catalog Number: 8435-1

Flower Orthopedics

Class I - Dangerous

Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery unless a second set is available

Nov 2, 2021 Other Medical Devices Nationwide View Details →