Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141 Access Point Medical Canes, Cane, Off-Set Crook w/Strap-Black, Product Code CN10051, packaged 20/case. The responsible firm is Access Point Medical, St. Louis, MO. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Access Point Medical Canes, Cane, Off-Set Crook w/Strap-Black, Product Code CN10051, packaged 20/case. The responsible firm is Access Point Medical, St. Louis, MO.
Brand
Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141
Lot Codes / Batch Numbers
All canes bearing the model number.
Products Sold
All canes bearing the model number.
Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141 is recalling Access Point Medical Canes, Cane, Off-Set Crook w/Strap-Black, Product Code CN10051, packaged 20/cas due to The canes were made of unacceptable materials and could break. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The canes were made of unacceptable materials and could break
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026