🔍 RecallPedia

REF S313152 Straight Acetabular Inserter Handle Ringloc non-sterile Orthopedic manual surgical instrument

Class I - Dangerous
🏥 Medical Devices Recalled: February 5, 2013 Biomet Surgical Instruments

What Should You Do?

  1. Check if you have this product:
    Catalog Number 5313152 Lot 153880,153930, 415500, 648010
  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:
Biomet, Inc.
Reason for Recall:
The Straight Ringloc Button Latch Inserter Handle may have been manufactured at the higher end of the tolerance causing interference with the Ringloc cup. The inserter handle may lock onto the cup during impaction. If alternative inserters are not available this could cause a surgical delay greater than 30 minutes.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

REF S313152 Straight Acetabular Inserter Handle Ringloc non-sterile Orthopedic manual surgical instrument

Product Codes/Lot Numbers:

Catalog Number 5313152 Lot 153880,153930, 415500, 648010

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0925-2013

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