Arjo Disposable Repositioning Sling — Class II medical device recall Z-2470-2021
Terminated recall by Getinge Dominican Republic SA, reported 2021-09-22, distributed nationwide. Sling loop straps on device pose a trip hazard.
| Recall number | Z-2470-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Getinge Dominican Republic SA, Itabo, Haina, N/A, Dominican Republic (the) |
| Recall initiated | 2021-07-30 |
| Classified | 2021-09-13 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2023-08-11 |
| Distributed | Nationwide (US) |
| Quantity | 46,085 units |
| Lot numbers | DAG1300482, DAG1300483, DAG1300484, DAG1300485, DAG1300486, DAG1300487, DAG1300522, DBG1300488, DBG1300489, DBG1300490, DBG1300491, DBG1300492, DBG1300493, DBG1300494, DBG1300495, DBG1300496, DBG1300497, DBG1300498, DBG1300499, DCG1300500, DCG1300501, DCG1300502, DCG1300503, DCG1300504, DCG1300505, DCG1300506, DCG1300507, DCG1300508, DCG1300509, DCG1300510, DCG1300511, DCG1300513, DCG1300514, DCG1300515, DDG1300516, DDG1300517, DDG1300518, DDG1300519, DDG1300520, DDG1300521 and 15 more |
| Model numbers | AHD001 |
Product
Arjo Disposable Repositioning Sling, Model AHD001
Reason for recall
Sling loop straps on device pose a trip hazard.
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-2470-2021. 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.