Z-0812-03

Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS

Name: Z-0812-03 Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS
Creator: Action Products Incorporated
Published: 2003-02-25
License: https://open.fda.gov/license/

Action Products, Inc. / initiated 2003-02-25 / Terminated

FDA source

Action Products Incorporated began a recall of Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS on 2003-02-25. The reason FDA records is "Stitching in wheelchair seat back is defective and may not support user". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0812-03
Status: Terminated
Initiated: 2003-02-25
Posted: 2003-05-14
Terminated: 2003-07-07
Recalling firm: Action Products, Inc.
Product: Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS.
Product code: IOR Wheelchair, Mechanical
Reason for recall: Stitching in wheelchair seat back is defective and may not support user.
FDA root cause: Other
Action: Firm notified dealers and sales representatives by certified letter on 2/25/03. Dealers were requested to phone the company for replacement options. Sales representatives were advised of the stitching failure via an 'urgent product recall' letter and instructed to immediately cease use and distribution, and further notify customers. Reps were asked to collect all recalled parts WPHS from consignees they have identified and return with response form.
Quantity in commerce: 40 units
Distribution: Product was distributed to dealers, independent sales representatives, and distributors around the US and worldwide.
Product codes and lots: LOTS IA702, II327, IK454, IM236

Product code IOR

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)