🔍 RecallPedia

aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use.

Class I - Dangerous
🏥 Medical Devices Recalled: January 11, 2019 AAP Implantate Ag Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: I011, I012, I013, I014, I015, I016, I017
  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:
AAP Implantate Ag
Reason for Recall:
There is the potential for the Lambotte chisel to break at the welded piece parts of the chisel body and knocking plate.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use.

Product Codes/Lot Numbers:

Lot Numbers: I011, I012, I013, I014, I015, I016, I017

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1019-2019

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