Arjo Flat Dynamic Positioning System — Class II medical device recall Z-1100-2021
Terminated recall by Arjohuntleigh Magog, Inc., reported 2021-02-17, distributed nationwide. Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS)
| Recall number | Z-1100-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arjohuntleigh Magog, Inc., Magog, N/A, Canada |
| Recall initiated | 2020-10-06 |
| Classified | 2021-02-09 |
| Reported by FDA | 2021-02-17 |
| Terminated | 2025-07-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, CA, CZ, FR, IT, PL |
| Quantity | 3,390 units |
| Reason classes | device malfunction |
Product
Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed for resident transfer in a homecare setting, at nursing homes and other assisted living centers. Please note that the DPS can be utilized only if affixed to ceiling lift or passive floor lift.
Reason for recall
Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS)
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-1100-2021. 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.