Events

Recall of Device Recall Access Point Quad Cane

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Access Point Medical LLC.

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
    35920
  • Event Risk Class
    Class 2
  • Event Number
    Z-0205-2007
  • Event Initiated Date
    2006-03-10
  • Event Date Posted
    2006-11-22
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2008-04-24
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=47152
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    cane - Product Code IPS
  • Reason
    The canes were made of unacceptable materials and could break.
  • Action
    The firm began making telephone calls and issuing recall letters dated 3/9/06 via UPS on 3/10/06. The telephone call explained the reason for recall and notified the customer they would be receiving a letter requesting return of the canes. The letter additionally notified the customer the recall was to be affected to the retail level. A customer response form was enclosed. The firm issued a second recall letter dated 12/22/06 via registered mail on 12/26/06 explaining the reason for recall, pointing out the hazard involved with the use of the recalled canes, and requesting they cease sales of the product. The letter requested they notify their customers of the recall and to post the enclosed recall placard where it can be seen by returning customers. Recall instructions were enclosed outlining step-by-step instructions for their customer to follow, including destroying the canes on site. A Customer Response Form was also enclosed. The firm issued a third letter dated 1/11/07 via regular mail which included a corrected placard because the product code numbers were incorrect in the placard included with the letter dated 12/22/06. The customers were instructed to discard the previous placard.

Device

Device Recall Access Point Quad Cane
  • Model / Serial
    All canes bearing the model number.
  • Product Classification
    Physical Medicine Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    Access Point Medical Canes, Quad Cane, Large Base - Gold, Product Code CN11070B, and Large Base - Chrome, Product Code CN11070C, both packaged 6/case. The responsible firm on the label is Access Point Medical, St. Louis, MO.
  • Manufacturer
    Access Point Medical LLC

Manufacturer

Access Point Medical LLC
  • Manufacturer Address
    Access Point Medical LLC, Three City Place Drive, Suite 750, St. Louis MO 63141
  • Source
    USFDA