Z-0205-2007

Access Point Medical Canes, Quad Cane, Large Base - Gold, Product Code CN11070B, and Large Base - Chrome...

Name: Z-0205-2007 Access Point Medical Canes, Quad Cane, Large Base - Gold, Product Code CN11070B, and Large Base - Chrome...
Creator: Access Point Medical LLC
Published: 2006-03-10
License: https://open.fda.gov/license/

Access Point Medical, LLC / initiated 2006-03-10 / Terminated

FDA source

Access Point Medical LLC began a recall of Access Point Medical Canes, Quad Cane, Large Base - Gold, Product Code CN11070B, and Large Base - Chrome, Product Code CN11070C, both packaged 6/case. The... on 2006-03-10. The reason FDA records is "The canes were made of unacceptable materials and could break". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0205-2007
Status: Terminated
Initiated: 2006-03-10
Posted: 2006-11-22
Terminated: 2008-04-24
Recalling firm: Access Point Medical, LLC
Product: 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.
Product code: IPS Cane
Reason for recall: The canes were made of unacceptable materials and could break
FDA root cause: Other
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.
Quantity in commerce: 63/6-cane cases
Distribution: Nationwide.
Product codes and lots: All canes bearing the model number.

Product code IPS

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)