Lower riskMedical device recall · FDA · Published June 10, 2021
Arjo Citadel Beds with IndiGo Modules Risk Power Cord Damage - Recall
Arjo Citadel beds made between May 2018 and February 2021 with IndiGo modules may have power cords that wear, potentially causing cuts, burns, or short circuits. Affected units include specific model numbers and retrofitted kits.
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.
Take action
Contact the company
📍Recalling firmARJOHUNTLEIGH POLSKA Sp. z.o.o.Ul. Ks. Piotra Wawrzyniaka 2 · Komorniki, Poland
“Arjo Citadel Beds with IndiGo Modules Risk Power Cord Damage - Recall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62352-arjo-citadel-beds-with-indigo-modules-risk-power-cord-damage. Based on FDA recall #Z-2588-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2588-2021%22&limit=1).
The FDA announced on June 10, 2021, that ARJOHUNTLEIGH POLSKA Sp. z.o.o. is recalling Arjo Citadel beds and IndiGo modules due to a fire hazard. The power cord may wear, leading to damage, burning, or short circuits with limited spark emission. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Arjo
Product: Arjo Citadel beds originally assembled with IndiGo modules during manufacturing; IndiGo modules (retrofit kits)
Model numbers: CX812A3J3AMAD0 (beds); INDIDAA (Citadel retrofit); INDIJAA (Enterprise retrofit)
Manufacturing dates: 5/25/2018-2/15/2021
Distribution: US Nationwide in CA, FL, IL, KY, MD, NV, NY, PA, and SD
Units affected: 367
The hazard
According to the FDA, the IndiGo power cord might wear during use, which could lead to its damage. This damage could result in the cord being cut, burnt, or short-circuited with limited emission of sparks.
Context
GovInfoNow's records show ARJOHUNTLEIGH POLSKA Sp. z.o.o. has 6 other recalls on record since 2018-10-22. Other recent recalls include the Arjo Tenor Patient Lift Recall (2026-03-10), Arjo Medical Beds Recall (2023-08-29), and Sara Plus Active Floor Lift Recall (2022-04-05). Other recent recalls of similar products include the Medline Semi Electric Lightweight Bed Recall (2025-11-26) and Maquet PowerLED 300 Concealed Lighting System Recall (2026-08-07).
How to tell if you have this one
Check for the model number CX812A3J3AMAD0 on the bed or IndiGo module. Also, look for the model numbers INDIDAA or INDIJAA on beds retrofitted with IndiGo modules. Manufacturing dates range from May 25, 2018, to February 15, 2021.
Brand
Arjo
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Power Cord Condition
Inspect the power cord for signs of wear, cuts, or burns. If damaged, stop using the bed immediately.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 9 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of CA, FL, IL, KY, MD, NV, NY, PA, and SD.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Illinois, Kentucky, Maryland, Nevada, New York, Pennsylvania, South Dakota.
Recall timeline
FDA terminated this recall 4.7 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2588-2021 (June 10, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2588-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.