ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland
Lot Codes / Batch Numbers
Serial number range: P0597830 to P0610470 Model numbers: FXX21A4A4AKFBB, FXX21A4D3AMFBA, FXX21C4B1AAABB, FXX21C4B4ABQBA, FXX21A4C4ACGBB, FXX21A4A1ABUBA, FXX21A6C2ABPBB, FXX21C4B1AAABA, FX811B3B4AMABB, FXX21C4D4AKBBB, FX611A2B2ALVBB
Products Sold
Serial number range: P0597830 to P0610470 Model numbers: FXX21A4A4AKFBB, FXX21A4D3AMFBA, FXX21C4B1AAABB, FXX21C4B4ABQBA, FXX21A4C4ACGBB, FXX21A4A1ABUBA, FXX21A6C2ABPBB, FXX21C4B1AAABA, FX811B3B4AMABB, FXX21C4D4AKBBB, FX611A2B2ALVBB
ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland is recalling Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute an due to Modular Junction Box (MJB) cables can melt and affect the bed functionality.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Modular Junction Box (MJB) cables can melt and affect the bed functionality.
Recommended Action
Per FDA guidance
On July 21st 2020 the firm, ARJO, sent an "URGENT-FIELD SAFETY NOTICE" notification to their US customers indicating the following: Although the likelihood of a serious injury is limited, (as the specific sequence of events is necessary), Arjo is taking this matter very seriously and intends to perform corrective action on the affected units. Next Steps 1. Verify whether you possess devices within the range of this Notice and ensure that all caregivers and users of Arjo Citadel Plus beds are made aware of this Field Safety Notice (FSN). If you do not use Skin IQ mattress, check the position of the Skin IQ cable (situated at the footend of the bed). In order to mitigate the risk of electric shock occurrence, protect the cable connector against touching, e.g by hiding it under the mattress. If Skin IQ mattress is being used (is connected via cable) no risk of electrick shock is present. 3. Ensure that the device does not stay in use if the malfunction occurs (control panels starts blinking, the functionality of the bed is disturbed, unpleasant smell is emitted), until the repair is performed. 4. Complete and sign the enclosed Customer Response Form and return this form to your local Arjo office; Fax: 1-833-329-2756, email:mailto:ArjoCustomer.Response-US@Arjo.com or mail: Arjo Inc., 2349 W Lake St. #250, Addison IL 60101. Once returned, Arjo will contact the designated facility representative listed on the Customer Response Form to schedule the service visit and repair all affected devices at your facility. In situations where Arjo is already aware of number of impacted units at your location, Arjo will offer immediate repair or swap to avoid any logistical inconvenience to our customers. Note: if your facility has sold or moved affected Citadel Bed, please include the new facilitys information in the Customer Response Form. The notice has been submitted to the Regulatory Agency/National Competent Authority in your country. If you have any furth
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026