🔍 RecallPedia

Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT

Class I - Dangerous
🏥 Medical Devices Recalled: January 13, 2022 Nextremity Solutions Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 1574701, 158961 UDI: 00817701026372
  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:
Nextremity Solutions
Reason for Recall:
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT

Product Codes/Lot Numbers:

Lot Numbers: 1574701, 158961 UDI: 00817701026372

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0740-2022

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