Events

Recall of DRILLS QUICK-CONNECT

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by ZIMMER BIOMET CANADA INC..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    143627
  • Event Risk Class
    II
  • Event Initiated Date
    2017-06-01
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    Zimmer biomet is recalling various trauma and extremity instruments because of a raw material anomaly. the anomaly has the potential to be on or below the surface and can increase the risk of instrument fracture. accordingly all products manufactured with the affected raw material are being removed from the field.

Device

DRILLS QUICK-CONNECT
  • Model / Serial
    Model Catalog: 00-2410-040-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-035-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-027-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-015-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-025-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-021-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-020-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 00-2410-026-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 02.00024.325 (Lot serial: 63385956); Model Catalog: 00-2255-031-37 (Lot serial: 63485036); Model Catalog: 00-2255-031-37 (Lot serial: 63485033); Model Catalog: 00-4807-230-25 (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 00-4807-195-45 (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 00-4807-180-25 (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 00-4806-195-32 (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 00-4806-145-45 (
  • Product Description
    ECT INTERNAL FRACTURE FIXATION QUICK-CONNECT DRILL;NCB PERIPROSTHETIC PLATE SYSTEM DRILL BIT;M/DN INTRAMEDULLARY FIXATION FEMORAL DRILLS;FRACTURE DRILLS - DRILL BIT;HERBERT BONE SCREW;M/DN INTRAMEDULLARY FIXATION SYSTEM FEMORAL DRILL;ZIMMER NATURAL NAIL S
  • Manufacturer
    ZIMMER BIOMET CANADA INC.

Manufacturer

ZIMMER BIOMET CANADA INC.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Zimmer Biomet Holdings
  • Manufacturer comment
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    HC