Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog… — Class II medical device recall Z-1308-2026
Ongoing recall by ETAC A/S, reported 2026-02-11, distributed nationwide. A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting
| Recall number | Z-1308-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ETAC A/S, Gedved, N/A, Denmark |
| Recall initiated | 2025-11-17 |
| Classified | 2026-02-05 |
| Reported by FDA | 2026-02-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CH, CZ, DE, ES, FI, FR, GB, IL, IT, JP, NO, NZ, PL, QA, SE |
| Quantity | 95 units |
| UPC / GTIN / UDI-DI | 05707995032270 |
| Serial numbers | 584307, 584501, 585701, 585801, 585802, 585803, 585804, 585805, 585806, 585807, 585808, 585809, 585810, 585811, 590801, 590901, 590902, 590903, 590904, 590905, 590906, 591001, 591002, 591003, 591004 and 70 more |
| Model numbers | M14000, M14001, M1401, M1402, M1402-01, M14050, M14050-00, M14150 |
Product
Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050, (5) M14150, (6) M1402-01, (7) M14050-00 (8) M14001;
Reason for recall
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
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-1308-2026. 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.