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    Architect Sirolimus Reagent Pack; 100 test pack containing 1 bottle (8.0 mL) Anti-Sirolimus Coated Microparticles, 1 bottle (8.0 mL) Sirolimus Acridinium-labeled Conjugate in Citrate Buffer, and 1 bottle (10 mL) Assay Diluent containing saline; Abbott Laboratories, Abbott Diagnostics Division, Abbott Park, IL 60064 USA; list 01L76-25. The Architect Sirolimus assay is chemiluminescent microparticle immunoassay (CMIA) for the quantitative determination of sirolimus in human whole blood on the Architect i System, as an aid in the management of renal transplant patients receiving sirolimus therapy.

    FDA Recall
    Terminated ·Abbott Laboratories·Product code NRP·May 27, 2010

    Toshiba Aquilion ONE CT SystemTSX-301 A/2D

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·February 3, 2009

    Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping (1.4GHz) Product Number: 865350 Exchange part: 453564262491 453564262511 453564615311 453564615331 453564262571 453564262591 USA only SW Revisions: B.05.28, B.05.29, and B.05.32 Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals

    FDA Recall
    Terminated ·Philips Electronics North America Corporation·Product code MHX·September 19, 2016

    Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product Number: 865352 Exchange part: 453564262491 453564262511 453564615311 453564615331 453564262571 453564262591 Exchange part: 453564262531 453564262551 453564262571 453564262591 453564615351 453564615371 453564467761 (Korea) 453564467781 (Korea) 453564451791 (Japan, Taiwan, Indonesia) 453564451811 (Japan, Taiwan, Indonesia) 453564467821 (Mexico) 453564467841 (China) 453564467861 (China) Worldwide SW Revisions: B.05.28, B.05.29, and B.05.32 Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals

    FDA Recall
    Terminated ·Philips Electronics North America Corporation·Product code MHX·September 19, 2016

    Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping (2.4GHz) Product Number: 865351 Worldwide Except USA Exchange part: 453564262491 453564262511 453564615311 453564615331 453564262571 453564262591 Exchange part: 453564262531 453564262551 453564262571 453564262591 453564615351 453564615371 453564467761 (Korea) 453564467781 (Korea) 453564451791 (Japan, Taiwan, Indonesia) 453564451811 (Japan, Taiwan, Indonesia) 453564467821 (Mexico) 453564467841 (China) 453564467861 (China) Worldwide except for the USA SW Revisions: B.05.28, B.05.29, and B.05.32 Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals

    FDA Recall
    Terminated ·Philips Electronics North America Corporation·Product code MHX·September 19, 2016

    Norian Drillable Inject 5 CC-Sterile; catalog # 07.704.005S Intended for bony voids or defects of the extremities and pelvis that are not instrinsic to the stability of the bony structure.

    FDA Recall
    Terminated ·Synthes (USA) Products LLC·Product code MQV·May 11, 2016

    Norian Drillable Inject 3 CC-Sterile; catalog # 07.704.003S Intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure.

    FDA Recall
    Terminated ·Synthes (USA) Products LLC·Product code MQV·May 11, 2016

    Norian Drillable Inject 10 CC-Sterile; catalog # 07.704.010S Intended for bony voids or defects of the extremities and pelvis that are not instrinsic to the stability of the bony structure.

    FDA Recall
    Terminated ·Synthes (USA) Products LLC·Product code MQV·May 11, 2016

    Victory Motorized Vehicle, 3 wheel Model SC1600

    FDA Recall
    Terminated ·Pride Mobility Product Corp·Product code INI·July 1, 2004

    Victory Motorized Vehicle 4 wheels Model SC1700

    FDA Recall
    Terminated ·Pride Mobility Product Corp·Product code INI·July 1, 2004

    Chauffeur Powered Scooters.

    FDA Recall
    Terminated ·Electric Mobility Corp·Product code INI·February 7, 2003

    Electric Mobility Corporation (EMC)- Scooters and Turnabout Powerchairs with either an Electric Seat Lift Actuator or a Seat Post to attach the seat to the vehicle; Model Number(s) 300F, 600C, 600T, and 600F. Electronic Mobility Corporation, 599 Mantua Blvd, One Mobility Plaza, Sewell, NJ 08080

    FDA Recall
    Terminated ·Electric Mobility Corp·Product code INI·March 22, 2007

    Medline Strider Midi 4 Scooter; a four wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mudelein, IL 60060 USA; model MDS807550 - red and MDS807550B - blue

    FDA Recall
    Terminated ·Medline Industries Inc·Product code INI·July 20, 2006

    Medline Strider Maxi 4 Scooter; a four wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807650 - red and MDS807650B - blue

    FDA Recall
    Terminated ·Medline Industries Inc·Product code INI·July 20, 2006

    Rascal LiteWay 214 manufactured by Giant Manufacturing, Taiwan.

    FDA Recall
    Terminated ·Electric Mobility Corp·Product code INI·September 27, 2010

    Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.

    FDA Recall
    Terminated ·Pride Mobility Products Corp·Product code INI·November 26, 2010

    Gyrus ACMI, REF 25 BX, PTFE Coated 3 cm Flexible Tip Guidewire, .035" x 150 cm, Sterile EO, Rx Only, Gyrus ACMI, Inc. 136 Turnpike Road,Southborough, MA 01772-2104 USA Ureteral guidewires are used to establish access in the urinary system for the passage of urological devices. An introducer is first used to establish entry to various portions of the urinary tract (urethra, bladder, ureter), then a guidewire is threaded through the introducer. Following placement of the guidewire, various urological devices can be introduced into the targeted portion of the urinary tract for various therapeutic and diagnostic procedures.

    FDA Recall
    Terminated ·Gyrus Acmi, Incorporated·Product code KNY·April 15, 2011

    Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue

    FDA Recall
    Terminated ·Medline Industries Inc·Product code INI·July 20, 2006

    Rascal UltraLite 370B manufactured by Giant Manufacturing, Taiwan.

    FDA Recall
    Terminated ·Electric Mobility Corp·Product code INI·September 27, 2010

    Rascal Powered Scooters.

    FDA Recall
    Terminated ·Electric Mobility Corp·Product code INI·February 7, 2003