Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Enterprise 9000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to ArjoHuntleigh has received reports of unintended movement where...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Arjo, Inc. dba ArjoHuntleigh directly.
Affected Products
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, care of the elderly, HDU, ITU, coronary care and oncology. The bed is appropriate for high dependency patients who pose a movement and handling risk and/or whose clinical condition requires that they are positioned with the minimal physical handling.
Quantity: 1,324 beds in USA, 138 beds in Canada, 1,877 beds ROW
Why Was This Recalled?
ArjoHuntleigh has received reports of unintended movement where the backrest and/or thigh sections of the bed have moved without anyone consciously pressing the control button. These incidents have occurred in High Dependency and Intensive Therapy environments where unintended movement of the patient may have serious consequences.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Arjo, Inc. dba ArjoHuntleigh
Arjo, Inc. dba ArjoHuntleigh has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report