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  • Device 13259
  • Manufacturer 13259
  • Event 13553
  • Implant 0
Name Date Date initiated Country Source
Recall of FLOWPRA CLASS I AND II SCREENING TESTS 2009-09-30 Canada HC
Recall of SCLEROTHERAPY INJECTION NEEDLES 2005-12-20 Canada HC
Recall of BIOMEDICAL TELEMETRY SYSTEM 1995-10-02 Canada HC
Recall of GEM ACTIVE CAN ELECTRODE IMPLANTABLE CARDIOVERTER/DEFIBRILLATOR 2001-01-08 Canada HC
Recall of MISYS LABORATORY MICROBIOLOGY 2003-07-16 Canada HC
Recall of TRINICLOT APTT HS REAGENT 2009-07-03 Canada HC
Recall of GEM ACTIVE CAN ELECTRODE IMPLANTABLE CARDIOVERTER/DEFIBRILLATOR 1999-08-10 Canada HC
Recall of STRAUMANN ORTHO SYSTEM - PALATAL IMPLANT SYSTEM - PALATAL IMPLANT TI 2008-07-28 Canada HC
Recall of CLASSIC STERISORB STERILE ABSORBENT PAD 2018-01-29 Canada HC
Recall of RIGIFLEX II ACHALASIA BALLOON DILATOR 2006-04-13 Canada HC
Recall of EPIC NITINOL BILIARY STENT SYSTEM 2008-04-11 Canada HC
Recall of ARROW POWER SERIES WHEELCHAIR 2003-03-06 Canada HC
Recall of AVALON FETAL MONITOR FM20 - MAIN UNIT 2009-06-10 Canada HC
Recall of THERMASPLINT KITS (COMES IN SMALL MEDIUM AND LARGE) 2011-06-17 Canada HC
Recall of CORN MEAL AGAR W/ POLYSORBATE 80 2005-01-25 Canada HC
Recall of MEDI-MAN PATIENT LIFTER 1995-09-19 Canada HC
Recall of ACCESS SYSTEM - TOTAL BHCG ASSAY 2001-04-24 Canada HC
Recall of STREP A TWIST RAPID TEST DEVICE 2011-09-26 Canada HC
Recall of ACCU-CHEK ADVANTAGE TEST STRIPS 2006-03-01 Canada HC
Recall of TEXIUM CLOSED MALE LUER WITH FEMALE CAP 2007-10-11 Canada HC
Recall of MAGNETOM VISION MRI 2002-11-14 Canada HC
Recall of ECLIPSE Canada HC
Recall of MAGNETOM TRIO 2004-04-02 Canada HC
Recall of SKYTRON 3502 EZ SLIDE SURGICAL TABLE 2016-10-04 Canada HC
Recall of BY-PASS PACK 2015-06-22 Canada HC
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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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