Arjo Portable Scale Adaptor — Class II medical device recall Z-1629-2023
Ongoing recall by Arjohuntleigh Magog, Inc., reported 2023-05-31, distributed in NY, OH. Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
| Recall number | Z-1629-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arjohuntleigh Magog, Inc., Magog, N/A, Canada |
| Recall initiated | 2023-02-17 |
| Classified | 2023-05-24 |
| Reported by FDA | 2023-05-31 |
| Distributed | NY, OH |
| Quantity | 3 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 05055982760713 |
| Serial numbers | 300501841, 300501842, 300515661 |
| Model numbers | 700.05725 |
Product
Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Reason for recall
Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1629-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.