---
title: "Sit to Stand STS500 Patient Lift — FDA record Z-1205-2023 | Is It on Recall"
description: "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."
url: https://isitonrecall.com/recall/fda-device-z-1205-2023-sit-to-stand-sts500-patient-lift/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Sit to Stand STS500 Patient Lift — FDA record Z-1205-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 3, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **Classification**: Class II
- **Recalling firm**: Med-Mizer, Inc.
- **Quantity**: 37 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1205-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1205-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Awaiting consignee list from the recalling firm.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Mar 8, 2023
- **Recall initiation date**: Feb 3, 2023
- **Center classification date**: Mar 2, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1205-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Med-Mizer, Inc. records](https://isitonrecall.com/brand/med-mizer-inc/)