ZOLL AED Pro External Defibrillator 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/Silver Spring: 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:

EU issues 42 Product, Toy & Vehicle Recalls

Belgium/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:

Lifepak 1000 Defibrillator Field Action [US]

US/Silver Spring: 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:

TUSA Dive Computer Recall [US]

US/Washington: TUSA 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.

Interlogix Panic Alarm Recall [Canada]

Canada/Ottawa: Interlogix 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).

Argos Mamas & Papas Car Seat Recall [UK]

UK/Basildon: Argos recalls certain batch/lots of Mamas & Papas Car Seats sold due to possible operational failure and consequential child injury hazard. CTSI: http://ht.ly/XGEq300IaB5

Direct link: http://www.tradingstandards.uk/advice/advice-recall-item.cfm?id=316071

Additional information:
The UK Chartered Trading Standards Institute (“CTSI”) reports the following Car Seats are subject to this recall: