FDA Device recall Z-1352-2019
Molift 2-Point sling bar, an accessory for Molift Mover 180/Air
- 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 180/Air 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-1352-2019 |
| 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 180/Air. Item nos. 1830001 1830002 1830002C 1830003
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-1352-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.