FDA Device recall Z-2588-2021
Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0
- FDA Device
- Class II
- terminated
- Published 2021-10-06
On 2021-10-06 the FDA classified a Class II recall of Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0 by Arjohuntleigh Polska Sp Z O O, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2588-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-06-10 |
| Published | 2021-10-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Arjohuntleigh Polska Sp Z O O |
| Distribution | US |
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
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.
Identifiers
| code_info | Manufacturing dates 5/25/2018-2/15/2021 (printed on both the bed and IndiGo module if the module was assembled on the b…Manufacturing dates 5/25/2018-2/15/2021 (printed on both the bed and IndiGo module if the module was assembled on the bed at the time of manufacture, or printed on the module if it was later installed on the bed. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Arjohuntleigh Polska Sp Z O O
- Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
FDA Device · Class II · 2026-04-22 · Arjohuntleigh Polska Sp Z O O - Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module a…
FDA Device · Class II · 2024-01-03 · Arjohuntleigh Polska Sp Z O O - Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module a…
FDA Device · Class II · 2024-01-03 · Arjohuntleigh Polska Sp Z O O - Sara Plus Active Floor Lift
FDA Device · Class I · 2022-06-01 · Arjohuntleigh Polska Sp Z O O - Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments
FDA Device · Class II · 2020-08-26 · Arjohuntleigh Polska Sp Z O O
All Arjohuntleigh Polska Sp Z O O recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2588-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.