🔍 RecallPedia

EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ adjust aluminum crutch, tall adult, 1 pair per case & 6) EZ adjust aluminum crutch, tall adult, 8 pairs per case

Class I - Dangerous
🏥 Medical Devices Recalled: February 17, 2016 Medical Depot Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Item #: 1) 10430-1, 2) 10430-8, 3) 10431-1, 4) 10431-8, 5) 10432-1 & 6) 10432-8
  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:
Medical Depot Inc.
Reason for Recall:
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ adjust aluminum crutch, tall adult, 1 pair per case & 6) EZ adjust aluminum crutch, tall adult, 8 pairs per case

Product Codes/Lot Numbers:

Item #: 1) 10430-1, 2) 10430-8, 3) 10431-1, 4) 10431-8, 5) 10432-1 & 6) 10432-8

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2102-2016

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