Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of ArjoLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Arjohuntleigh Magog with 6 device recalls. The most recent is a device recall dated Feb 17, 2023: Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in co….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 17, 2023 | Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipmentClass II · Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach. | Device recalls |
| Mar 4, 2021 | Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring functionClass II · The spreader bar can disconnect from the scale bottom attachment. | Device recalls |
| Oct 6, 2020 | Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed for resident transfer iClass II · Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS) | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
