BEUDAMED
    89 results · 21ms · Sources: EU EUDAMED, US FDA

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    UNO 100 EM/EE Patient Lift

    FDA Recall
    Terminated ·Liko, Inc.·Product code FNG·September 24, 2004

    Penner Manufacturing Patient Transfer/Lift System, Cascade Transfer, Models 380000-1 (white) and 380000-2 (gray). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Pacific Chair with scale, Patient Transfer/Lift System, Models 394000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Bariatric Patient Transfer/Lift System, Cascade Transfer, Models 382500-1 (right entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Pacific Chair, Patient Transfer/Lift System, Models 393000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Superior end entry with scale, Patient Transfer/Lift System, Models 389000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Superior end entry, Patient Transfer/Lift System, Models 386000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Sabina I and II EM/EE Patient Lift

    FDA Recall
    Terminated ·Liko, Inc.·Product code FNG·September 24, 2004

    Penner Manufacturing Transfer Electric Bariatric with Scale, Patient Transfer/Lift System, Cascade Transfer, Models 383500-1 (right entry with scale). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Superior right entry, Patient Transfer/Lift System, Models 384000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Cascade Patient Transfer/Lift System, Models 382000-1 (right entry) and 382000-1L (left entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    BHM Medical Infrared (IR) Hand Control System, an optional wireless control component of the Arjo Maxi Sky 600 and BHM V4 Ceiling Patient Lifts; the hand control system is composed of two components, part 700.13640.33 - IR hand control, and part 492.00038 - IR receiver board

    FDA Recall
    Terminated ·Arjo, Inc.·Product code FNG·February 20, 2008

    Minstrel Patient Lift with SR weighing scale; a non-AC-powered patient lift; Arjo, Inc., 50 N. Gary Ave., Roselle, IL 60172; model number HMB002-US

    FDA Recall
    Terminated ·Arjo, Inc.·Product code FNG·August 31, 2006

    Penner Manufacturing Transfer Electric Superior left entry with scale, Patient Transfer/Lift System, Models 388000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    Penner Manufacturing Transfer Electric Cascade with Scale, Patient Transfer/Lift System, Models 383000-1 (right entry) and 383000-1L (left entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    JASMINE Full Body (Patient) Lift, electrically-powered device with a 500 lb. weight capacity. The recalled product is an electrically-powered device either fixed or mobile, used to lift and transport patients in the horizontal or other required position from one place to another.

    FDA Recall
    Terminated ·Invacare Corporation·Product code FNG·April 1, 2011

    Penner Manufacturing Transfer Electric Superior left entry, Patient Transfer/Lift System, Models 385000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009

    BHM Combi Sling, 100% Polyester Shell/100% Polyester Strap; soft polyester net fabric sling for ceiling and floor patient lifts; BHM, Magog, Canada, made in China. Part 626002: Combi Deluxe - Medium, capacity 68-113 kg, 150-250 lbs; Part 626002M: Combi Mesh Deluxe - Medium, capacity 68-113 kg, 150-250 lbs; Part 626002C Combi Sling Deluxe Small, capacity 20-68 kg, 45-150 lbs; Part 626002C-M Combi Sling Mesh Deluxe Small, capacity 20-68 kg, 45-150 lbs; Part 626003: Combi Deluxe - Large, capacity 113-272 kg, 250-600 lbs; Part 626003M: Combi Mesh Deluxe - Large, capacity 113-272 kg, 250-600 lbs; and Part 626003X: Combi Oversize Heavy Duty, capacity 113-272 kg, 250-600 lbs. Between 2004 and 2006, the Combi Slings were labeled as BHM Medical Inc. (800) 868-0441, 100% Polyester Shell/100% Nylon Strap, made in Canada. Prior to 2004, the slings were labeled Medi-Man, 100% Polyester Shell, Rehabilitation Products Inc., Mississauga, Ontario, Canada L5T 1X7, made in Canada. The accessory is intended to be used with patient lift for the transfer of patient in hospitals, nursing homes, or other health care facilities by trained caregivers.

    FDA Recall
    Terminated ·B.H.M. Medical, Inc.·Product code FNG·April 7, 2009

    UNO 102 EM/EE/ES Patient Lift

    FDA Recall
    Terminated ·Liko, Inc.·Product code FNG·September 24, 2004

    Penner Manufacturing Transfer Electric Superior right entry with scale, Patient Transfer/Lift System, Models 387000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.

    FDA Recall
    Terminated ·Penner Mfg Inc·Product code FNG·January 19, 2009