Molift 2-Point sling bar — Class II medical device recall Z-1351-2019
Ongoing recall by Moller Vital, reported 2019-05-22, distributed in AZ, DE, FL, GA, MA, OH, SC, TX…. The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially
| Recall number | Z-1351-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Moller Vital, Gjovik, Norway |
| Recall initiated | 2019-02-04 |
| Classified | 2019-05-16 |
| Reported by FDA | 2019-05-22 |
| Distributed | AZ, DE, FL, GA, MA, OH, SC, TX, WA, WI |
| Countries outside the US | AU, CA |
| Quantity | 427 total |
| Reason classes | device malfunction |
| Model numbers | 1430016, 1430017, 1430021 |
Product
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
Reason for recall
The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.
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-1351-2019. 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.