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FDA Medical Device Recalls (openFDA)

Action Products Incorporated: Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS.

Recall number
Z-0812-03
Recalling firm
Action Products Incorporated
Product
Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS.
Status
Terminated
Initiated
2003-02-25
Posted
2003-05-14
Terminated
2003-07-07
Reason
Stitching in wheelchair seat back is defective and may not support user.
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
40 units
Distribution
Product was distributed to dealers, independent sales representatives, and distributors around the US and worldwide.
Lot, serial or model codes
LOTS IA702, II327, IK454, IM236
510(k) numbers
not on file
PMA numbers
not on file
Product code
IOR
Firm FEI
1181047
Firm city
Hagerstown
Firm state
MD
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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