Devices

Device Recall Baxter

  • Modèle / numéro de série
    All DiscPac products are affected within expiry up to October 2017
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.
  • Manufacturer
    Baxter Corporation Englewood
  • 1 Event

Fabricant

Baxter Corporation Englewood
  • Adresse du fabricant
    Baxter Corporation Englewood, 14445 Grasslands Dr, Englewood CO 80112-7062
  • Société-mère du fabricant (2017)
    Baxter International
  • Source
    USFDA

155 dispositifs médicaux avec un nom similaire

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Device Recall Baxter FloGard 6201 Volumetric Infusion Pumps
  • Modèle / numéro de série
    product code 2M8063, serial numbers 312424FB, 401424FB, 402089FB, 405111FB, 406060FB, 406067FB, 406154FB, 406155FB, 410334FB, 504036FB, 504053FB, 504061FB,  504378FB, 505328FB, 5090200FB, 5120672FB, 5120673FB, 6010044FB, 6050216FB, 7090392FB, 72000920, 72002220, 7202164Y, 7202357Y, 73041636, 73043106, 73044076, 73045746, 73048047, 73048607, 8070182FB, 93001467, 93007507, 10010241FB, 10100618FB, 10100652FB,  11010414FB, 11030373FB, 11050043FB, 11050487FB, 11050505FB, 11060149FB, 12060080FB, 13020041FB, 13040040FB, 13090060FB, 14020080FB, 13050172FB, 14080040FB.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide: Alaska, Arizona, California, Colorado, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Kansas, Kentucky, Louisiana, Maryland, Michigan, Mississippi, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Washington and Wyoming
  • Description du dispositif
    Baxter Flo-Gard 6201, SIngle Channel , Volumetric Infusion Pump; Baxter Healthcare Corporation, Deerfield, IL 60015; Product Code # 2M8063
  • Manufacturer
    Baxter Healthcare Corp.
Device Recall Baxter FloGard 6301 Dual Channel Volumetric Infusion Pumps
  • Modèle / numéro de série
    product code 2M8064, serial numbers RA00449, RA00771, RA01093, RA01103FA, RA01143, RA01212FA, RA01241FA, RA01352, RA01392, RA01471FA, 4020417FA, 4110026FA, 4110599FA, 4111648FA, 5010398FA, 5010588FA, 5010892FA, 5030542FA, 5031363FA, 5041317FA, 5041836FA, 5050032FA, 5101954FA, 5111071FA, 5111215FA, 5111217FA, 6020538FA, 6051302FA, 6110083FA, 6110621FA, 6110976FA, 6112818FA, 6113536FA, 6120726FA, 6120952FA, 6121014FA, 6121201FA, 6121249FA, 62004506, 62009976,62013806, 62020266, 62067349, 62069349, 6208698X, 63106801, 63111022, 63111672, 63157766, 63159996, 63173758, 7120494FA, 8020914FA, 8030070FA, 8060094FA, 8080471FA, 8090732FA, 8090762FA, 8111587FA, 8111640FA, 83003592, 83039198, 83044518, 83055250, 83064210, 83069140, 9030584FA, 9030593FA, 9110819FA, 10091327FA, 10091426FA,10091428FA, 10110600FA, 10111225FA, 10111396FA, 10112596FA, 10113463FA, 10113550FA, 10113557FA, 10120142FA, 11030108FA, 11030281FA, 11030908FA, 11031331FA, 11042552FA, 11042740FA, 11042815FA, 11051333FA, 11052654FA, 11052741FA, 11052809FA, 11052957FA, 11061064FA, 11070997FA, 11072099FA, 11081754FA, 11100082FA, 11111119FA, 11120281FA, 11120313FA, 11120327FA, 11120346FA, 12020834FA, 12010409FA, 12031733FA, 12040163FA, 12041054FA, 12060362FB, 12060972FA, 12061359FA, 12061727FA, 12070800FA, 12080863FA, 12090274FA, 12100402FA, 12101819FA, 12102195FA, 12102656FA, 12102742FA, 12102862FA, 12120472FA, 12121033FA, 13010030FA, 13010283FA, 13070260FA, 13070316FA, 13080047FA, 13100967FA, 13101196FA, 13110190FA, 14010668FA, 14050871FA, 14071117FA, 14071128FA, 14071153FA, 14071166FA, 14091581FA, 14091796FA, 14020391FA, 14020002FA, 15013155FA, 15013208FA, 15050126FA, 15050608FA.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide: Alaska, Arizona, California, Colorado, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Kansas, Kentucky, Louisiana, Maryland, Michigan, Mississippi, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Washington and Wyoming
  • Description du dispositif
    Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pump; Baxter Healthcare Corporation, Deerfield, IL 60015; Product code # 2M8064
  • Manufacturer
    Baxter Healthcare Corp.
Device Recall Baxter Single Day INFUSOR System
  • Modèle / numéro de série
    Lot Numbers: 07E037, 07E038, 07E039, 07E055, 07E056, 07E057, 07F015, 07F029, 07F030, 07F039, 07G003, 07G004, 07G043, 07H004, 07H005, 07H006, 07H035, 07H036, 07H037, 07H057, 07H059, 07H061, 07H074, 07J016, 07J018, 07J052, 07J054, and 07K020
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide: USA, Canada, Austria, Belgium, Denmark, Finland, France, Germany, Greece, Italy, Portugal, San Marino, Spain, Sweden, United Kingdom, South Africa, Colombia, Argentina, Hong Kong, Australia and New Zealand.
  • Description du dispositif
    Baxter Single Day INFUSOR Portable Elastomeric Infusion System, Product Code: 2C1071KJP; 2mL/hr with Tubing Flow Restrictor; 12 units per case; Baxter Healthcare Corporation, Deerfield, IL 60015
  • Manufacturer
    Baxter Healthcare Corp.
Device Recall Baxter Minicap Extended Life PD Transfer Set (6")with Twist Clamp
  • Modèle / numéro de série
    Product code 5C4482, lot number H09E19059.
  • Classification du dispositif
    Gastroenterology-Urology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US (states of Arkansas, Illinois, Mississippi, North Carolina, Tennessee and Virginia) and El Salvador.
  • Description du dispositif
    Baxter Minicap Extended Life PD Transfer Set (6") with Twist Clamp; six sets per carton; Baxter Healthcare Corporation, Deerfield, IL 60015 USA; product code 5C4482 The set is used in disconnect applications and cycler applications where aseptic connections and disconnections are performed at the transfer set/cycler juncture.
  • Manufacturer
    Baxter Healthcare Corp.
Device Recall Baxter Minicap Extended Life PD Transfer Set Extra SHort (4") with Twist Clamp
  • Modèle / numéro de série
    Product code 5C4483, lot number H09E18044.
  • Classification du dispositif
    Gastroenterology-Urology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US (states of Arkansas, Illinois, Mississippi, North Carolina, Tennessee and Virginia) and El Salvador.
  • Description du dispositif
    Baxter Minicap Extended Life PD Transfer Set Extra Short (4") with Twist Clamp; six sets per carton; Baxter Healthcare Corporation, Deerfield, IL 60015 USA; product code 5C4483 The set is used in disconnect applications and cycler applications where aseptic connections and disconnections are performed at the transfer set/cycler juncture.
  • Manufacturer
    Baxter Healthcare Corp.
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