FDA Medical Device Recalls (openFDA)
Rehabilicare: Line Powered RePak, Model Number 1785S
- Recall number
- Z-0931-03
- Recalling firm
- Rehabilicare
- Product
- Line Powered RePak, Model Number 1785S
- Status
- Terminated
- Initiated
- 2003-05-23
- Posted
- 2003-06-17
- Terminated
- 2004-07-02
- Reason
- If there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse.
- Root cause
- Other
- Action
- Recall letters dated May 21, 2003 requested that consignees return the product and a response form to the firm. Distributors were requested to recall the product from their customers.
- Quantity
- 618 Line Powered RePaks
- Distribution
- Nationwide in the United States
- Lot, serial or model codes
- Line Powered RePaks, Model Number 1785S, distributed from April 9, 2003 to May 7, 2003 are to be recovered. Between 04/09/03 and 05/07/03, 618 Line Powered RePaks (Model 1785S) were shipped.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GZJ
- Firm FEI
- 2126518
- Firm city
- New Brighton
- Firm state
- MN
- 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