FDA Medical Device Recalls (openFDA)
Arjohuntleigh Magog, Inc.: Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
- Recall number
- Z-1629-2023
- Recalling firm
- Arjohuntleigh Magog, Inc.
- Product
- Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
- Status
- Open, Classified
- Initiated
- 2023-02-17
- Posted
- 2023-05-24
- Terminated
- not on file
- Reason
- Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
- Root cause
- Process control
- Action
- Arjo issue an URGENT MEDICAL DEVICE RECALL notice to its consignees on 02/17/2023 via letter, UPS, 2nd Day Delivery. The notice explained the problem, the risk, and requested the consignee remove the units from use and destroy them. The firm will be replacing the units upon receipt of the completed response form. For questions or assistance in completing the Customer Response Form, please contact Arjo at 1 800-323-1245 or via email at ArjoCustomer.Response-US@arjo.com.
- Quantity
- 3
- Distribution
- US: OH, NY
- Lot, serial or model codes
- UDI/DI 05055982760713, Serial Numbers: 300501841, 300501842, 300515661
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 3002655016
- Firm city
- Magog
- Firm state
- not on file
- Firm country
- Canada
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