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Revised instructions for use Recalls in Canada
17 recalls involving revised instructions for use — most are medical devices recalls. Newest first, updated daily from government open data.
Showing 1–17 of 17
Mega 2000™ and Mega Soft™ Patient Return Electrodes - Potential Risk of Patient Burn Injuries
Revised instructions for use - Labelling and packaging - Increased risk or new adverse events
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Nim™ Standard Reinforced Emg Endotracheal Tube & Nim Contact™ Reinforced Emg Endotracheal Tube
Revised instructions for use
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Intelepacs
Revised instructions for use
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Xvivo Organ Chamber
Revised instructions for use
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Negative Pressure Wound Therapy Sved Device
Revised instructions for use
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Ellex Tango Reflex and Ultra Q Reflex devices
Revised instructions for use
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Dabir System
Revised instructions for use
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Exalt Model D Single-Use Duodenoscope
Revised instructions for use
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Spaceoar System
Revised instructions for use
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Temperature Probes
Revised instructions for use
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Magec 1
Revised instructions for use
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Heartware Ventricular Assist System
Revised instructions for use
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Precice System
Revised instructions for use
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BIOGRAPH MCT
Revised instructions for use
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BIOGRAPH LSO 16 SLICE PET
Revised instructions for use
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Miami J Select Cervical Collar
Revised instructions for use
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Ocean Chest Drain
Revised instructions for use
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