Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame… — Class II medical device recall Z-2821-2020
Terminated recall by ARJOHUNTLEIGH POLSKA Sp. z.o.o., reported 2020-08-26, distributed nationwide. Modular Junction Box (MJB) cables can melt and affect the bed functionality.
| Recall number | Z-2821-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o., Komorniki, N/A, Poland |
| Recall initiated | 2020-07-21 |
| Classified | 2020-08-18 |
| Reported by FDA | 2020-08-26 |
| Terminated | 2021-02-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BR, CA, DE, FR |
| Quantity | 145 units |
| Model numbers | FX611A2B2ALVBB, FX811B3B4AMABB, FXX21A4A1ABUBA, FXX21A4A4AKFBB, FXX21A4C4ACGBB, FXX21A4D3AMFBA, FXX21A6C2ABPBB, FXX21C4B1AAABA, FXX21C4B1AAABB, FXX21C4B4ABQBA, FXX21C4D4AKBBB |
Product
Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments. It is not intended for use in the home care environment.
Reason for recall
Modular Junction Box (MJB) cables can melt and affect the bed functionality.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2821-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.