FDA Device recall Z-1205-2023
Sit to Stand STS500 Patient Lift
- FDA Device
- Class II
- ongoing
- Published 2023-03-08
On 2023-03-08 the FDA classified a Class II recall of Sit to Stand STS500 Patient Lift by Med Mizer, citing risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1205-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-03 |
| Published | 2023-03-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Med Mizer |
| Distribution | n/a |
Product
Sit to Stand STS500 Patient Lift
Reason
Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.
Identifiers
| code_info | UDI-DI: 00852195007353; Serial No.: STS500000, STS500001, STS500002, STS500003, STS500004, STS500005, STS500006, STS500…UDI-DI: 00852195007353; Serial No.: STS500000, STS500001, STS500002, STS500003, STS500004, STS500005, STS500006, STS500007, STS500008, STS500009, STS500010, STS500011, STS500012, STS500013, STS500014, STS500015, STS500016, STS500017, STS500018, STS500019, STS500020, STS500021, STS500022, STS500023, STS500024, STS500025, STS500026, STS500027, STS500028, STS500029, STS500030, STS500031, STS500032, STS500033, STS500034, STS500035, and STS500036. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1205-2023%22
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