---
title: "NOA Medical Industries Behavioral Health Hospital bed side rails, Product num... — FDA record Z-0838-2025 | Is It on Recall"
description: "Red button used to engage side rails can break or become stuck making it difficult to engage the side rail."
url: https://isitonrecall.com/recall/fda-device-z-0838-2025-noa-medical-industries-behavioral-health-hospital-bed-side-rails-product-number-1055050gry-box/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX — FDA record Z-0838-2025

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 Nov 5, 2024. 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**: NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX
- **Reason**: Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
- **Classification**: Class II
- **Recalling firm**: NOA Medical Industries Inc
- **Quantity**: 34 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0838-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0838-2025%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 00817492012745, Serial Numbers: 2038043534, 2038042756, 2038042755, 2038042750, 2038042751, 2038042752, 2038042753, 2038042754, 2038042757, 2038042244, 2038041722, 2038038738, 2038038750, 2038038749, 2038038748, 2038038747, 2038038746, 2038038745, 2038038744, 2038038758, 2038038757, 2038038756, 2038038754, 2038038753, 2038038752, 2038038755, 2038038743, 2038038742, 2038038737, 2038038751, 2038038739, 2038038740, 2038038741, 2038038766. |

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

## Distribution

US: GA, MI. MA, CA

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

- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Michigan](https://isitonrecall.com/state/michigan/)

## Dates in the source

- **Report date**: Jan 22, 2025
- **Recall initiation date**: Nov 5, 2024
- **Center classification date**: Jan 10, 2025

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-0838-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [NOA Medical Industries Inc records](https://isitonrecall.com/brand/noa-medical-industries-inc/)