Triangle Tube Prestige Gas Boiler Recall [US & Canada]

Triangle Tube Prestige Condensing Gas Boilers Recall [US & Canada]

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US FlagCanada FlagUS/Washington & Canada/Ottawa: Triangle Tube/III Co., Inc., a West Deptford, New Jersey establishment recalls an estimated total of 69,600 Prestige Solo & Prestige Excellence Condensing Gas Boilers (approximately 63,000 in the US and approximately 6,600 in Canada) from the American and Canadian marketplaces due to possible Vent Adapter detachment and consequential risks of Carbon Monoxide poisoning, respiratory depression, nausea, confusion, cardiac arrhythmia, seizures and death, all serious health and safety hazards.

CPSC: http://ht.ly/Tm0l30r2VjI; HCSC: http://ht.ly/VyjO30r2VjL

Direct US link: https://www.cpsc.gov/Recalls/2020/Triangle-Tube-Recalls-to-Repair-Gas-Boilers-Due-to-Risk-of-Carbon-Monoxide-Hazard-One-Death-Reported-In-Home-Remedy-May-Be-Delayed-Due-To-COVID-19-Restrictions

Direct Canada link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73415r-eng.php

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves twenty-two (22) models of the Prestige Solo & Prestige Excellence Condensing Gas Boiler manufactured between November 2011 and October 2019 sold, marketed and installed for residential and light commercial use.

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Becca Cosmetics Light Shifter Concealer Recall [Canada]

Becca Cosmetics Light Shifter Concealer Recall [US]

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Canada FlagCanada/Ottawa: Becca Cosmetics, a New York, New York establishment, and American subsidiary of Becca Cosmetics, of Perth, Australia and part of the Estée Lauder Group of companies recalls certain batch/lots of Becca Cosmetics branded Light Shifter Brightening Concealer products from the Canadian marketplace due to suspected Mould contamination and consequential risks of skin irritation, allergy, Keratitis, Endophthalmitis and/or possible life-changing complications including eye damage and/or blindness, all serious health and safety hazards.

HCSC: http://ht.ly/fnQf30qSRfw

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73397r-eng.php

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

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Becca Cosmetics Light Shifter Concealer Recall [US]

Becca Cosmetics Light Shifter Concealer Recall [US]

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US FlagUS/Silver Spring: Becca Cosmetics, a New York, New York establishment, and American subsidiary of Becca Cosmetics, of Perth, Australia and part of the Estée Lauder Group of companies recalls certain batch/lots of Becca Cosmetics branded Light Shifter Brightening Concealer products from the American marketplace due to suspected Mold contamination and consequential risks of skin irritation, allergy, Keratitis, Endophthalmitis and/or possible life-changing complications including eye damage and/or blindness, all serious health and safety hazards.

FDA: http://ht.ly/qEy730qE6z4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/becca-cosmetics-voluntarily-recalls-light-shifter-brightening-concealer

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

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Accutome, Focus Ointment, Grandall & Prestige Eye Drops

US FlagUS/Silver Spring: Logo - Altaire PharmaAltaire Pharmaceuticals Inc, an Aquebogue, New York establishment, recalls certain batch/lots of multiple Ophthalmic (Eye) Drop, Gel and Ointment products sold by various third-party companies including Accutome, Focus Laboratories, Grandall Distributing and Prestige due to possible non-sterility and/or consequential risks of bacterial, viral or mold infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/82sg30p9QdA

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/altaire-pharmaceuticals-inc-issues-voluntary-recall-multiple-over-counter-ophthalmic-products-sold

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

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