Events

Recall of PERCUTANEOUS NEPHROSTOMY CATHETERS WITH LOOP LOCKING RETENTION

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BOSTON SCIENTIFIC LTD..

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
    25223
  • Event Risk Class
    III
  • Event Initiated Date
    2009-03-30
  • 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
    During the attempted removal of the device sutures were separated from the catheter and remained in the patient. in one instance surgical intervention was opted to remove a suture.

Device

PERCUTANEOUS NEPHROSTOMY CATHETERS WITH LOOP LOCKING RETENTION
  • Model / Serial
    Model Catalog: 410-111 (Lot serial: >100 SEE FILE); Model Catalog: 410-112 (Lot serial: >100 SEE FILE); Model Catalog: 410-126 (Lot serial: >100 SEE FILE); Model Catalog: 410-204 (Lot serial: >100 SEE FILE); Model Catalog: 410-205 (Lot serial: >100 SEE FILE); Model Catalog: 410-202 (Lot serial: >100 SEE FILE); Model Catalog: 410-206 (Lot serial: >100 SEE FILE); Model Catalog: 410-305 (Lot serial: >100 SEE FILE); Model Catalog: 410-304 (Lot serial: >100 SEE FILE); Model Catalog: 410-203 (Lot serial: >100 SEE FILE); Model Catalog: 410-207 (Lot serial: >100 SEE FILE)
  • Product Description
    PERCUTANEOUS COMBINATION STENT
  • Manufacturer
    BOSTON SCIENTIFIC LTD.

Manufacturer

BOSTON SCIENTIFIC LTD.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Boston Scientific
  • Manufacturer comment
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    HC