Maxi Sky 1000 — Class II medical device recall Z-2479-2021
Terminated recall by Arjohuntleigh Magog, Inc., reported 2021-09-22, distributed in AZ, CA, CO, IL, LA, MA, MI, MO…. The spreader bar can disconnect from the scale bottom attachment.
| Recall number | Z-2479-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arjohuntleigh Magog, Inc., Magog, N/A, Canada |
| Recall initiated | 2021-03-04 |
| Classified | 2021-09-16 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2024-01-12 |
| Distributed | AZ, CA, CO, IL, LA, MA, MI, MO, OH, PA, WA |
| Quantity | 62 units |
| Model numbers | 454, 700-00526, 700-00536 |
Product
Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function
Reason for recall
The spreader bar can disconnect from the scale bottom attachment.
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-2479-2021. 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.