---
title: "ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4 — FDA record Z-2271-2024 | Is It on Recall"
description: "The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issu"
url: https://isitonrecall.com/recall/fda-device-z-2271-2024-alphamaxx-mobile-operating-table-model-number-part-number-113322b4/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4 — FDA record Z-2271-2024

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 May 29, 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**: ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4
- **Reason**: The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
- **Classification**: Class II
- **Recalling firm**: Getinge Usa Sales Inc
- **Quantity**: 73 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2271-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2271-2024%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 | Model Number/Part Number: 113322B4; UDI/DI: 04046768040007; Serial Numbers: 3018 through 3078, 3080 through 3086, 3088 through 3089, 3095 through 3097. |

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

## Distribution

Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech Republic, Denmark, France, Greece, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Mexico, New Zealand, Norway, Poland, Romania, Saudi Arabia, South Africa, Spain, Switzerland, Thailand, United Arab Emirates, United Kingdom.

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

- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Jul 17, 2024
- **Recall initiation date**: May 29, 2024
- **Center classification date**: Jul 5, 2024

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-2271-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Getinge Usa Sales Inc records](https://isitonrecall.com/brand/getinge-usa-sales-inc/)