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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JYSK TINGI Super Glue Recall [Canada]

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TINGI Super Glue Recall [Canada]Canada/Ottawa: JYSK Linen ‘N Furniture Ltd., a Coquitlam, British Columbia establishment, recalls an estimated 1,301 tubes of TINGI branded Super Glue products due to suspected failure to meet child-resistant packaging requirements for quick skin-bonding adhesives required by Canada’s Consumer Chemicals and Containers Regulations, 2001 and consequential unintentional exposure to these adhesives, serious illness, ingestion, poisoning, injury and/or death, all serious health and safety hazards.

HCSC: http://ht.ly/tIOC30oVbsB

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70043r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves certain super glue products packaged in a blister pack and identified by a UPC of 6902244112645 and a product number of 11019-17-1010, as follows:

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Drip More Candy King Vaping Fluid Recall [US]

Drip More Candy King Vaping Fluid Recall [US]

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US FlagUS/Silver Spring: Drip More, LP, a Riverside, California establishment, recalls four (4) batch/lots for a total estimated 7,105 units of Candy King – Worms Vaping Fluid due to suspected elevated Nicotine content and consequential risk of Nicotine overdose including nausea, vomiting, rapid heart rate (“Tachycardia”), pale skin, headache, dizziness, confusion and seizures, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/JcuW30oTgxu

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/drip-more-lp-voluntarily-recalls-four-lots-candy-king-worms-3-mg-100-ml-due-elevated-nicotine

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

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PECGEN DMX Cough Syrup Recall [US]

PECGEN DMX Cough Syrup Recall [US]

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US FlagUS/Silver Spring: NOVIS PR LLC, a Rio Piedras, Puerto Rico establishment, recalls an estimated five (5) batch/lots of PECGEN DMX Cough Syrup due to suspected incorrect dosage information on its label and consequential risk of overdose producing seizures, coma and death, all serious health hazards.

FDA: http://ht.ly/XSof30oRByQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novis-pr-llc-issues-voluntary-nationwide-recall-pecgen-dmx-due-labeling-error

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

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EU issues 26 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 21/2019 of its Rapid Alert System containing 26 consumer, automotive and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/zusw30oPCJQ

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=3422&Year=2019&lng=en

Additional information:
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EU issues 37 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 20/2019 of its Rapid Alert System containing 37 consumer, automotive and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/JchN30oL4SH

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=3412&Year=2019&lng=en

Additional information:
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Libra 3-Drawer Dresser/Chest Recall [US, Canada & Mexico]

Libra 3-Drawer Dresser/Chest Recall [US, Canada & Mexico]

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Canada FlagMexico FlagUS FlagUS/Washington, Canada/Ottawa & Mexico/Mexico City: South Shore Furniture recalls approximately 322,500 Libra style 3-Drawer Dresser/Chests due to tip-over, entrapment and death, all serious safety hazards.

CPSC: http://ht.ly/TcxM30oH0Gr; HCSC: http://ht.ly/HQai30oH0Jn; PROFECO: not listed;

Direct US link: https://www.cpsc.gov/Recalls/2019/South-Shore-Furniture-Recalls-Chest-of-Drawers-Due-to-Serious-Tip-Over-and-Entrapment-Hazards-One-Fatality-Reported

Direct Canada link: https://www.cpsc.gov/Recalls/2019/South-Shore-Furniture-Recalls-Chest-of-Drawers-Due-to-Serious-Tip-Over-and-Entrapment-Hazards-One-Fatality-Reported

Direct Mexico link: not listed

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Libra style 3-drawer Dresser/Chests sold in nine colors.

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