ARJOHUNTLEIGH POLSKA Sp. z.o.o.: Medical Device Recall in 2020 - (Recall #: Z-2821-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: July 21, 2020

Date Posted: August 26, 2020

Recall Number: Z-2821-2020

Event ID: 86065

Reason for Recall:

Modular Junction Box (MJB) cables can melt and affect the bed functionality.

Status: Terminated

Product Quantity: 145 units

Code Information:

Serial number range: P0597830 to P0610470 Model numbers: FXX21A4A4AKFBB, FXX21A4D3AMFBA, FXX21C4B1AAABB, FXX21C4B4ABQBA, FXX21A4C4ACGBB, FXX21A4A1ABUBA, FXX21A6C2ABPBB, FXX21C4B1AAABA, FX811B3B4AMABB, FXX21C4D4AKBBB, FX611A2B2ALVBB

Distribution Pattern:

Worldwide distribution: US (nationwide) to states of:: FL, KS, LA and countries of:: Australia, Brazil, Canada, France and Germany.

Voluntary or Mandated:

Voluntary: Firm initiated