🔍 RecallPedia

Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU: NX-4532K-SC Orthopedic surgical instrument

Class I - Dangerous
🏥 Medical Devices Recalled: February 10, 2022 Nextremity Solutions Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Number: 168117318C, 168125017D UDI: 00817701020004
  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:
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU: NX-4532K-SC Orthopedic surgical instrument

Product Codes/Lot Numbers:

Lot Number: 168117318C, 168125017D UDI: 00817701020004

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0911-2022

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