---
title: "Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be... — FDA record Z-1629-2023 | Is It on Recall"
description: "Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach."
url: https://isitonrecall.com/recall/fda-device-z-1629-2023-arjo-portable-scale-adaptor-model-number-700-05725-accessory-intended-to-be-used-in-combination-with/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible pat... — FDA record Z-1629-2023

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 17, 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**: Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
- **Reason**: Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
- **Classification**: Class II
- **Recalling firm**: Arjohuntleigh Magog, Inc.
- **Quantity**: 3
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1629-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1629-2023%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 05055982760713, Serial Numbers: 300501841, 300501842, 300515661 |

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

## Distribution

US: OH, NY

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)

## Dates in the source

- **Report date**: May 31, 2023
- **Recall initiation date**: Feb 17, 2023
- **Center classification date**: May 24, 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-1629-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Arjohuntleigh Magog, Inc. records](https://isitonrecall.com/brand/arjohuntleigh-magog-inc/)