FDA Device recall Z-1351-2019
Molift 2-Point sling bar, an accessory for Molift Mover 205
- FDA Device
- Class II
- ongoing
- Published 2019-05-22
On 2019-05-22 the FDA classified a Class II recall of Molift 2-Point sling bar, an accessory for Molift Mover 205 by Moller Vital, citing 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 patien….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1351-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-02-04 |
| Published | 2019-05-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Moller Vital |
| Distribution | AZ, DE, FL, GA, MA, OH, SC, TX, WA, WI |
Product
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
Reason
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.
Identifiers
| code_info | All units manufactured between May 2013 and October 2018. Date of manufacture is labeled on the product. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1351-2019%22
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