Inogen One G3 Oxygen Concentrator Recall [Australia]

Australia FlagAustralia/Canberra: Logo - Air Liquide Healthcare Pty LtdAir Liquide Healthcare Pty Ltd, a Melbourne, Victoria establishment, recalls certain batch/lots of Inogen One G3 Concentrator Portable Lightweight Medical Oxygen Machines from the Australian marketplace due to suspected operational failure and consequential risk of oxygen supply loss, asphyxiation and death, all serious health and safety hazards.

ACCC: http://ht.ly/tq9D30qmtPY

Direct link: https://www.productsafety.gov.au/recall/air-liquide-healthcare-pty-ltd-inogen-one-g3-concentrator

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following At Home Oxygen Equipment products are subject to this recall:

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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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Allergan Taytulla Softgel Contraceptive Recall [US]

US FlagUS/Silver Spring: Taytulla Softgel Contraceptive Recall [US]Allergan plc, an Irvine, California establishment, recalls certain batch/lots of Taytulla Softgel Contraceptive (Birth Control) Capsules due to suspected presence of out-of-sequence Capsules and consequential risk of contraceptive failure and unintended pregnancy, all serious health and safety hazards.

FDA: http://ht.ly/oH2X30kfHEh

Direct link: https://www.fda.gov/Safety/Recalls/ucm609044.htm

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

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EU issues 42 Product, Toy & Vehicle Recalls

FlagEUBelgium/Brussels: The European Union issues Report 34-2017 of its Rapid Alert System containing 42 new consumer, automotive and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, supervisors and others: http://ht.ly/gwYD30eIx5f

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=2512&Year=2017

Additional information:
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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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TUSA Dive Computer Recall [US]

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US/Washington: 7783-tusadivecomputerTUSA recalls an estimated 175 Wrist-Mounted Dive Computers due to risk of operational failure and consequential drowning and decompression sickness hazards. CPSC: http://ht.ly/qBqs305BKJD

Direct link: https://www.cpsc.gov/Recalls/2017/TUSA-Recalls-Diving-Computers

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain TUSA DC Solar Link IQ1204 Dive Computer.

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Interlogix Panic Alarm Recall [Canada]

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Canada/Ottawa: 7498 - InterlogixPanicAlarmInterlogix recalls an estimated 2,500 Wireless Personal Panic Alarms due to operational failure hazard and consequential risk of non-communication in the event of an emergency. HCSC: http://ht.ly/foj1303DEEa

Direct link: http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/59170r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves certain Interlogix Wireless Personal Panic Devices, models TX-4200-01-1 (white in color with a UPC of 7-82136-72342-7) and TX-4200-01-2 (black in color with a UPC of 7-82136-72343-4).

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