Manufacturer

Arjo, Inc. dba ArjoHuntleigh

9 recalls in our database name Arjo, Inc. dba ArjoHuntleigh as the manufacturing or recalling firm.

What the numbers show

Total: 9
Critical: 0
Severe: 2
Most recent: 2017-07-19

Of the 9 recalls from Arjo, Inc. dba ArjoHuntleigh we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (22%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–9 of 9

HighFDA (Devices)·Z-2714-2017·2017-07-19
ArjoHuntleigh Flowtron ACS900 Medical Pump Recalled for Deflation Failure
Arjo, Inc. is recalling 40,675 Flowtron ACS900 medical pumps worldwide because the device may fail to deflate the calf garment as intended without triggering an alarm.
Product
ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff. Th
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1388-2016·2016-04-20
Arjo Concerto Basic Shower Trolley Recalled for Loose Bolts
Arjo is recalling 1,596 Concerto Basic Shower Trolleys because bolts connecting the stretcher to the hydraulic piston and tilting mechanism may become loose.
Product
The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents in care environments such as senior/assisted living, group home, special care, nursing homes, hospitals and home care. The Concerto Basic Shower Trolley is inten
Category
Medical Device
Distribution
36 states
HighFDA (Devices)·Z-0079-2015·2014-10-22
ArjoHuntleigh Recalls Spreader Bars for Ceiling Lifts Due to Hook Flexibility
Arjo, Inc. is recalling 363 spreader bars for the Maxi Sky 2 Ceiling Lift because the hooks are too flexible to securely hold sling loops.
Product
Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift; Model 700-19425. Intended to be used for general transfers in hospitals.
Category
Medical Device
Distribution
5 states
SevereFDA (Devices)·Z-0477-2013·2013-08-14
Arjo Enterprise 9000 Hospital Beds Recalled for Unintended Movement
ArjoHuntleigh is recalling Enterprise 9000 hospital beds because the backrest or thigh sections may move without user input, posing a risk to patients in high-dependency care.
Product
Enterprise 9000 Bed; an AC-powered adjustable hospital bed with built-in electronic weigh scale, patient bed exit alarm, and under bed anti-entrapment system; ArjoHuntleigh AB, Eslov, Sweden; Models 9000, 9600, 9700 and 9800 General medicine, general and specialist surgery, ca
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0476-2013·2013-08-14
ArjoHuntleigh Recalls Enterprise 8000 Hospital Beds Due to Unintended Movement
ArjoHuntleigh is recalling Enterprise 8000 hospital beds because the backrest or thigh sections may move without user input, posing a risk to patients in high-dependency care.
Product
Enterprise 8000 Bed; an AC-powered adjustable hospital bed; ArjoHuntleigh AB, Eslov, Sweden; Models 8000, 8001, 8002, 8003, 8500, 8600, 8700 and 8800 General medicine, general and specialist surgery, care of the elderly, HDU, ITU, coronary care and oncology. The bed is appropr
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2013·2013-01-02
Arjo Flowtron Trio DVT Pump Recalled for Lack of FDA Approval
Arjo, Inc. is recalling 2,859 Flowtron Trio DVT Pumps because they were marketed without proper FDA approval.
Product
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov, Sweden; Model 512003; a non-invasive prophylaxis system for reducing the incidence of deep vein thrombosis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1948-2012·2012-07-18
ArjoHuntleigh Recalls Chorus Mobile Patient Lifters Due to Injury Risk
ArjoHuntleigh is recalling specific Chorus Mobile Patient Lifters because an exposed metal support bracket can cause injuries when the knee pad assembly is removed.
Product
Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KKB5062-21US and KKB5080-21US. The Chorus is designed to be used as a standing and raising aid, it is useful for short transfers from one sit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1947-2012·2012-07-18
Arjo Encore Mobile Patient Lifter Recalled for Exposed Metal Bracket Injury Risk
ArjoHuntleigh is recalling specific Encore Mobile Patient Lifters because removing the knee pad assembly can expose a metal support bracket, posing an injury risk to patients.
Product
Encore Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5022-21US and KKB5042-21US. The Encore is designed to be used as a standing and raising aid, it is useful for short transfers from one sitting position
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1949-2012·2012-07-18
Arjo Sara Plus Patient Lifter Recalled for Exposed Metal Bracket Injury Risk
ArjoHuntleigh is recalling Sara Plus Mobile Patient Lifters because removing the knee pad assembly exposes a metal support bracket, posing an injury risk.
Product
Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel, Belgium; Models HEP0001-US and HEP1001-US. The Sara Plus is a standing and raising aid for short transfers e.g. raising from bed and transfer to wheelchair,
Category
Medical Device
Distribution
Distributed nationwide