# FDA recall Z-2588-2021

> **ARJOHUNTLEIGH POLSKA Sp. z.o.o.** · Class II · device recall initiated 2021-06-10.

## Product

Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0; and IndiGo modules (retrofit kits) that can be installed on Citadel (model no. INDIDAA) or Enterprise (model no. INDIJAA) beds manufactured without IndiGo modules assembled at the time of manufacturing and subsequently retrofitted on the beds.

## Reason for recall

The IndiGo power cord might wear during use which could lead to its damage, resulting in the cord being cut, burnt or short circuit with limited emission of sparks.

## Distribution

US Nationwide distribution in the states of CA, FL, IL, KY, MD, NV, NY, PA, and SD.

## Key facts

- **Recall number:** Z-2588-2021
- **Recalling firm:** ARJOHUNTLEIGH POLSKA Sp. z.o.o.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-10
- **Report date:** 2021-10-06
- **Termination date:** 2026-02-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Komorniki, N/A, Poland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2588-2021

## Citation

> AI Analytics. FDA recall Z-2588-2021. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2588-2021. Source: US FDA. Licensed CC0.

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