Lifepak 1000 Defibrillator Field Action [US]

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US/Silver Spring: Lifepak 1000 Defibrillator Field Action [US]Physio-Control issues a Voluntary Field Action for all current Lifepak 1000 Defibrillators due to suspected operational failure, unexpectedly shut-down during patient treatment and possible death, a serious health hazard. FDA: http://ht.ly/UI8o3080aAk

Direct link: http://www.fda.gov/Safety/Recalls/ucm537114.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Medical Devices are subject to this Field Action:

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MEC FilZer Lube Recall [Canada]

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Canada/Ottawa: MEC FilZer Lube Recall [Canada]Mountain Equipment Coop. (“MEC”) recalls an estimated 33,650 bottles of FilZer Lube Products due to suspected failure to provide the required child-resistant closures on its packaging and suspected failure to have proper hazard labelling required by the Consumer Chemicals and Containers Regulations, 2001 (“CCCR”, 2001) under the Canada Consumer Product Safety Act (“CCPSA”) and consequential ingestion and injury hazards. HCSC: http://ht.ly/525y30802e5

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/61756r-eng.php

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

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