Device Recall Overpressure Safety Valve

  • Modèle / numéro de série
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution: US, Canada, Colombia, UK, Belgium, and Japan
  • Description du dispositif
    Custom surgical kits containing TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 and (b) LH130J || Catalog numbers: || US distribution: || LH130 || 74369 || 71156 || 71551-02 || 71413 || 71692 || 74102 || 75490 || 74432-01 || 75477 || 75478 || 75104-02 || 75104-03 || 75477-01 || 75037 || 75973 || 75308-01 || 75688 || 70571-06 || 75114-01 || 72755 || 73306 || 71180-01 || 73307 || 75163 || 75164 || 75787 || 75163-01 || 73055-02 || 75450 || 75451 || 75452 || 75453 || 75453-01 || 75999 || 75451-01 || 72481-01 || 75197 || 73968 || 75416 || 73648 || 71519-02 || 71801-01 || 72846 || 74163-02 || 74178-03 || 74986 || 75607 || 74162-01 || 74163-03 || 73454-01 || 71296-01 || 74924 || 73344-04 || 73500-04 || 74924-01 || 73143-02 || 76393 || 74248-01 || 73820-01 || 75261 || 75594 || 74022-01 || 66001-01 || 66004-01 || 74916 || 72736-02 || B72736-02 || 70815 || 70815-01 || 70815-02 || 74356-02 || 73208-03 || 73001-02 || 73957-01 || 74460-01 || 70089-06 || 75168 || 75171 || 75240 || 74382-01 || 66467 || 70089-07 || 74965-03 || 75168-01 || 75240-01 || 66467-01 || 70089-08 || 73177 || 76006 || 73177-01 || 76038 || 75252-01 || 76316 || 75805-02 || 73346 || 76414 || 75790 || 75678 || 62007-01 || 66229 || 75075 || 62007-02 || 65382 || 75788 || 75788-01 || 70533-10 || 75936 || 75936-01 || 63123 || 72241 || 70148-02 || 70730 || 70772 || 74732 || 75090 || 75090-01 || 75090-02 || 75089-01 || 73468 || 74430 || 74921-02 || 75881 || 64523-02 || 64619-02 || 64522-03 || 64521-02 || 65560-03 || 64912-04 || 65560-04 || 71064 || 65570 || 71062-01 || 71061-02 || 71060-01 || 71962-04 || 71965-04 || 75948 || 71962-05 || 74401-01 || 74400-01 || 74399-02 || 75944 || 759
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Terumo Cardiovascular Systems Corporation, 125 Blue Ball Rd, Elkton MD 21921-5315
  • Société-mère du fabricant (2017)
  • Source
    USFDA

Un dispositif médical avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    SAFETY ALERT Lot Codes:  (a) RH14, RK11, RK20, RL02, RM06, RM20, RN10, RP08, TD16, TE13, TE27, TF14, TF21, TG04, TG11, TG17, TH06, TH16, TK10, TK24, TL08, TL21, TM28, TP14, UA11, UA18, UA25, UC08, UC22, UD14, UD21, UD28, UE05, UE18, UF09, UG06, UK01, UL12, UM10, UM31, UP05, VA02, VC06, VD06, VE10    (b) RH14, RH21, RK18, RL15, RM01, RM22, RN24, RP01, TA19, TF05, TF27, TG19, TH20, TK24, TL01, TM12, TN09, TP03, UA20, UC15, UD22, UE04, UE18, UF02, UG13, UH11, UK15, UL06, UM10, VA02, VA30, VC27, VE03, VF01   LH130 PRODUCT CORRECTION lot codes or serial number range: TA19 through VD06, distribution date range: 08Apr2015 through 20Jan2017
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution: US, Canada, Colombia, UK, Belgium, and Japan
  • Description du dispositif
    TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 (b) LH130J
  • Manufacturer