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Recall of NEWPORT BREEZE VENTILATOR
  • Type of Event
    Recall
  • Event ID
    132098
  • Event Risk Class
    II
  • Event Initiated Date
    1991-08-07
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of INTELLIGENT PUMP
  • Type of Event
    Recall
  • Event ID
    33345
  • Event Risk Class
    II
  • Event Initiated Date
    1992-04-03
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of ARTHRO-FLOW IRRIGATOR
  • Type of Event
    Recall
  • Event ID
    30748
  • Event Risk Class
    II
  • Event Initiated Date
    1992-10-28
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of LP10 VOLUME VENTILATOR
  • Type of Event
    Recall
  • Event ID
    23847
  • Event Risk Class
    II
  • Event Initiated Date
    1993-12-21
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
  • Type of Event
    Recall
  • Event ID
    127834
  • Event Risk Class
    II
  • Event Initiated Date
    1994-01-11
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of FLO-GARD 6301 DUAL-CHANNEL VOLUMETRIC INFUSION PUMP
  • Type of Event
    Recall
  • Event ID
    104711
  • Event Risk Class
    II
  • Event Initiated Date
    1994-01-11
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of AUTO SYRINGE INFUSION PUMP - MODEL AS50A
  • Type of Event
    Recall
  • Event ID
    25806
  • Event Risk Class
    III
  • Event Initiated Date
    1994-04-18
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of BLOOD WARMER *
  • Type of Event
    Recall
  • Event ID
    25580
  • Event Risk Class
    II
  • Event Initiated Date
    1994-07-20
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of VICRYL (POLYGLACTIN 910) ABSORBABLE SUTURES
  • Type of Event
    Recall
  • Event ID
    31874
  • Event Risk Class
    II
  • Event Initiated Date
    1994-09-14
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of KODAK MIN-R XRAY FILM
  • Type of Event
    Recall
  • Event ID
    69394
  • Event Risk Class
    II
  • Event Initiated Date
    1994-09-19
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of VITRECTOMY PACK *154660 154661
  • Type of Event
    Recall
  • Event ID
    79537
  • Event Risk Class
    II
  • Event Initiated Date
    1994-11-02
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of QUICK ABG SAMPLER
  • Type of Event
    Recall
  • Event ID
    85385
  • Event Risk Class
    II
  • Event Initiated Date
    1994-12-29
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    Mfr has determined that after use the needles have a potential for inadvertent withdrawal (backing out) from the stopper cube used for disposal. it is important that universal precautions be utilized for spec.
Recall of RESPONDER 1200 DEFIBRILLATOR
  • Type of Event
    Recall
  • Event ID
    130696
  • Event Risk Class
    I
  • Event Initiated Date
    1995-01-23
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of RESPONDER 1500
  • Type of Event
    Recall
  • Event ID
    43251
  • Event Risk Class
    I
  • Event Initiated Date
    1995-01-23
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of KODAK MIN-R XRAY FILM
  • Type of Event
    Recall
  • Event ID
    43310
  • Event Risk Class
    II
  • Event Initiated Date
    1995-01-26
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of CT 9000 CONTRAST DELIVERY SYSTEM - INJECTOR
  • Type of Event
    Recall
  • Event ID
    21149
  • Event Risk Class
    I
  • Event Initiated Date
    1995-02-21
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of STRATUS FMMZ DIGOXIN KIT
  • Type of Event
    Recall
  • Event ID
    32309
  • Event Risk Class
    III
  • Event Initiated Date
    1995-03-21
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of STRATUS FMMZ DIGOXIN KIT
  • Type of Event
    Recall
  • Event ID
    51873
  • Event Risk Class
    III
  • Event Initiated Date
    1995-03-24
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of BLOOD BANK QUALITY ASSURANCE TESTING REAGENTS
  • Type of Event
    Recall
  • Event ID
    31034
  • Event Risk Class
    III
  • Event Initiated Date
    1995-03-24
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of REVERSE-CYTE REAGENT RED BLOOD CELL
  • Type of Event
    Recall
  • Event ID
    19674
  • Event Risk Class
    III
  • Event Initiated Date
    1995-03-24
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of NEER 2 TOTAL SHOULDER METAL BACKED GLENOID
  • Type of Event
    Recall
  • Event ID
    49937
  • Event Risk Class
    II
  • Event Initiated Date
    1995-04-06
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of PARAMAX CSF/URINE PROTEIN REAGENT
  • Type of Event
    Recall
  • Event ID
    53236
  • Event Risk Class
    III
  • Event Initiated Date
    1995-05-01
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of MERCURIAL SPHYGMOMANOMETERS (BLOOD PRESSURE CUFFS)
  • Type of Event
    Recall
  • Event ID
    27266
  • Event Risk Class
    III
  • Event Initiated Date
    1995-06-08
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of FILSHIE CLIP SYSTEM
  • Type of Event
    Recall
  • Event ID
    84987
  • Event Risk Class
    II
  • Event Initiated Date
    1995-06-13
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
Recall of MEDI-MAN PATIENT LIFTER
  • Type of Event
    Recall
  • Event ID
    12359
  • Event Risk Class
    III
  • Event Initiated Date
    1995-09-19
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data