ZOLL AED Pro External Defibrillator Recall [Canada]

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ZOLL AED Pro External Defibillator Recall [Canada]

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Canada/Ottawa: ZOLL Medical Corporation, a Chelmsford, Massachusetts establishment, recalls an unknown number of ZOLL AED Pro External Defibrillators due to suspected component malfunction and consequential risk of operational failure and possible death during a cardiac event requiring defibrillation, all serious health hazards.

HCSC: http://ht.ly/gPNK30oXwCG

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70221r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Defibillator products are subject to this recall:

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Novopen Echo Insulin Device Recall [US]

US FlagUS/Silver Spring: Novopen Echo Insulin Device Recall [US]Novo Nordisk recalls certain batch/lots of Cartridge Holders for Novopen Echo Insulin Delivery Devices due to suspected risk of creaking and/or breakage and consequential Insulin delivery failure, Hyperglycemia and resultant life-threatening complications, all serious health hazards. FDA: http://ht.ly/Aquy30ds3rj

Direct link: https://www.fda.gov/Safety/Recalls/ucm565936.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following medical devices are subject to this recall:

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Venture Catheter Recall [US]

US FlagUS/Silver Spring: Logo - Venture CathetersVascular Solutions, Inc. recalls all batch/lots worldwide of Venture Catheters due to suspected extraneous material in the inner lumen of the distal Catheter tip and consequential component detachment or extrusion during use, embolism, serious injury and/or death hazards. FDA: http://ht.ly/Dkzn30d8YmD

Direct link: https://www.fda.gov/Safety/Recalls/ucm564419.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Catheters are subject to this recall (in alphanumeric order):

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Hospira Plum 360 Infusion Pump Recall [Canada]

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Canada/Ottawa: Hospira Plum 360 Infusion Pump Recall [Canada]Health Canada recalls certain batch/lots of Hospira Plum 360 Infusion Pumps running device software version 15.02 due to suspected operational failure and consequential interruption of any ongoing therapy and patient injury hazards. HCSC: http://ht.ly/NFHE307VXai

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/61738r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Infusion Pumps are subject to this recall:

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