Devices

Arrow

  • Model / Serial
    Product No. AP-06022. Lot Numbers: 12025, 12026, MF2082053, MF2092149, MF2102348, MF2112612, MF2112798, MF2122887, MF3013239, MF3023441, MF3033609, MF3033767, MF3043953, MF3054471, MF3054551, MF3064671, MF3064720, MF3074950, MF3075080, MF3085227, MF3085410, MF3106022, MF3126356, MF3116146, MF4020300, MF4020624, MF4031189, MF4041636, MF4041931, MF4052351, MF4063054, MF4063107, MF4063265, MF4073781, MF4073838, MF4105285, MF4105479, MF4105680, MF4126531, MF4126772, MF4126885, MF5017407, MF5028155, MF5038764, MF5050041, MF5059731, MF5059893, MF5060649, MF5081721, MF5082121, MF5092678. MF5103209, MF5103504, MF5113992, MF5114145, MF5124303, MF6015495, MF6036710, MF6047367, MF6047368, MF6057762, MF6058411, MF6068650, MS3110150, MS4041840.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide. The firm is NOT recalling from international accounts.
  • Product Description
    Implantable Vascular Access system -- Infusion Ports with Silicone Rubber Catheter. || Latex-Free Low Profile Port. 10 Fr. Introducer Kit || Ref Product No. AP-06022
  • Manufacturer
    Arrow International Inc
  • 1 Event

Manufacturer

Arrow International Inc
  • Manufacturer Address
    Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
  • Manufacturer Parent Company (2017)
    Teleflex Incorporated
  • Source
    USFDA

570 devices with a similar name

Learn more about the data here

Device Recall Bone Marrow Aspiration Needle
  • Model / Serial
    Lot Number 81351NDR
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide - FL, TX, WI, PA, MN, SC, NC, KY, TN, CA, AR, OR, NJ, and IA.
  • Product Description
    Angiotech, Bone Marrow Aspiration Needle, Medical Device Technologies, Inc. Individual packaged in blister pack. Packaged 10 per box. Sterile.
  • Manufacturer
    Medical Device Technologies, Inc.
Device Recall Bone Marrow Biopsy Needle
  • Model / Serial
    Lot Number 81371NGF and 81081MRM.
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide - FL, TX, WI, PA, MN, SC, NC, KY, TN, CA, AR, OR, NJ, and IA.
  • Product Description
    Angiotech, Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy.
  • Manufacturer
    Medical Device Technologies, Inc.
Device Recall TLOK Bone Marrow Biopsy Needle
  • Model / Serial
    Lot Number 81291N9Y
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide - FL, TX, WI, PA, MN, SC, NC, KY, TN, CA, AR, OR, NJ, and IA.
  • Product Description
    Angiotech, T-Lok Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy.
  • Manufacturer
    Medical Device Technologies, Inc.
Device Recall Arrow International, Inc. Intraaortic balloon catheter
  • Model / Serial
    Lot Number/Serial Numbers: MF7065606 MF7076012 MF7076021 MF7086462 MF7086736 MF7107536 MF7107537 MF7107694 MF7107696 MF7118048 MF7118049 MF7118050 MF7118151 MF7118221 MF7118222 MF7128472 MF7128506 MF7128507 MF8018908 MF8019033 MF8019034 MF8019035 MF8019104 MF8029191 MF8029433 MF8029434 MF8039774 MF8040251 MF8040287 MF8050764 MF8050812 MF8050966 MF8061267 MF8061413 MF8071676 MF8071863 MF8082268 MF8082507 MF8093002 MF8103280 MF8103416 MF8103571 MF8113836 MF8113919 MF8113951 and MF8124345.
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution: USA, Argentina, Australia, Taiwan, Singapore, New Zealand, India, Brazil, Belgium, Korea, Peru, Finland, and Denmark.
  • Product Description
    8 Fr 40cc Ultra 8 IAB, || IAB-05840-U, Intra-aortic balloon catheter. || The Intra-aortic balloon (IAB) is utilized for IAB counter-pulsation therapy, whereby balloon inflation in the aorta during diastole and deflation during systole increase blood supply to the heart muscle and decrease work of the left ventricle.
  • Manufacturer
    Arrow International, Inc.
Device Recall Arrow International, Inc. Intraaortic balloon catheter
  • Model / Serial
    Lot/Serial Numbers: MF6079580 MF6100954 MF7033668 MF7086558 MF7086984 MF7097225 MF7097426 MF7118000 MF7118001 MF7128557 and MF8018922.
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution: USA, Argentina, Australia, Taiwan, Singapore, New Zealand, India, Brazil, Belgium, Korea, Peru, Finland, and Denmark.
  • Product Description
    8 Fr 30cc Narrow Flex IAB Catheter Kit with Generica Adapters || Product Number: IAB-04830-U, Intra-aortic balloon catheter. || The Intra-aortic balloon (IAB) is utilized for IAB counter-pulsation therapy, whereby balloon inflation in the aorta during diastole and deflation during systole increase blood supply to the heart muscle and decrease work of the left ventricle.
  • Manufacturer
    Arrow International, Inc.
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