Abba Medix Sage N Sour Dried Cannabis Recall [Canada]

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Abba Medix Sage N Sour Dried Cannabis Recall [Canada]

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Canada/Ottawa: Abba Medix Corp., a Pickering, Ontario establishment, recalls an estimated 72 units of Sage N Sour Dried Cannabis products from the Canadian marketplace due to reported failure to properly identify the active cannabinoid values for THC and Total THC in a single batch/lot of the medication and consequential risks of THC impairment, decreased ability to operate machines and disorientation, all serious health and safety hazards.

HCSC: http://ht.ly/cakO30rfQz6

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/74027r-eng.php

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

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Holland & Barrett Super Hair Food Supplement Recall [UK]

Holland & Barrett Super Hair Food Supplement Recall [UK]

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UK FlagUK/London: Holland & Barrett, a Nuneaton, Warwickshire establishment, recalls certain batch/lots of Super Hair Food Supplement 1-A-Day Formula Tablets from the British marketplace due to undeclared Soya, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FSA: http://ht.ly/EdN330r7zQs

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-aa-47-2020

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Dietary Supplement products are subject to recall:

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Taro-Dermovate & Taro-Clobetasol Cream Recall [Canada]

Canada FlagCanada/Ottawa: Logo - Taro Pharmaceuticals IncTaro Pharmaceuticals Inc, a Brampton, Ontario establishment and subsidiary of Taro Pharmaceutical Industries Ltd. of Haifa, Israel recalls certain batch/lots of Taro-Dermovate Cream and Taro-Clobetasol Cream USP from the Canadian marketplace due to suspected product mixing irregularities and consequential risk of failure to meet content uniformity standards with possible under- and/or over-dose administration, all serious health and safety hazards.

HCSC: http://ht.ly/myJ930r1o7K

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73615r-eng.php

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

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Ferring DDAVP Drug Spray Recall [Canada]

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Ferring DDAVP Drug Spray Recall [Canada]

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Canada/Ottawa: Ferring Pharmaceuticals Inc., a Toronto, Ontario establishment, recalls certain batch/lots of DDAVP Spray (Desmopressin Acetate Nasal solution, 10 micrograms/spray) because the product may contain a higher than labelled dose of the active ingredient (Desmopressin), a consequential risk of drug overdose, a serious health hazard.

HCSC: http://ht.ly/jYQ030r07uq

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73567a-eng.php

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

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Ferring DDAVP Drug Spray Recall [Canada]

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Ferring DDAVP Drug Spray Recall [Canada]

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Canada/Ottawa: Ferring Pharmaceuticals Inc., a Toronto, Ontario establishment, recalls certain batch/lots of DDAVP Spray (Desmopressin Acetate Nasal solution, 10 micrograms/spray) because the product may contain a higher than labelled dose of the active ingredient (Desmopressin), a consequential risk of drug overdose, a serious health hazard.

HCSC: http://ht.ly/4KXF30qZhLh

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73575r-eng.php

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

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EU issues 28 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 25/2020 of its Rapid Alert System containing twenty eight (28) consumer, automotive, commercial 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/nClr30qSbyo

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=26&Year=2020&lng=en

Additional information:
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GSK Children’s Dimetapp & Robitussin Recall [US]

GSK Dimetapp & Robitussin Recall [US]

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US FlagUS/Silver Spring: GSK Consumer Healthcare, a Warren, New Jersey establishment, recalls two batch/lots of Children’s Robitussin Honey Cough and Chest Congestion DM and one lot of Children’s Dimetapp Cold and Cough from the American marketplace due to suspected inclusion of incorrect dosing cups and consequential risks of medication overdose and/or medication under-dosage, all serious health hazards.

FDA: http://ht.ly/bC3e30qRUAQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gsk-consumer-healthcare-issues-voluntary-nationwide-recall-childrens-robitussinr-honey-cough-and

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

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EU issues 33 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 24/2020 of its Rapid Alert System containing thirty three (33) consumer, automotive, commercial 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/Ul6b30qPoLQ

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=25&Year=2020&lng=en

Additional information:
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Teva Carvedilol Tablet Recall [Canada]

Canada FlagCanada/Ottawa: Logo - Teva Canada Ltd.Teva Canada Ltd., a Toronto, Ontario establishment, recalls certain batch/lots of Teva Carvedilol Tablets from the Canadian marketplace due to suspected oversize tablets and consequential risks of choking, oral injury, and GI tract laceration damage, all serious safety hazards.

HCSC: http://ht.ly/fvOo30qPoh6

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73325r-eng.php

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

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EU issues 31 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 23/2020 of its Rapid Alert System containing thirty one (31) consumer, automotive, commercial 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/z8Fz30qMYox

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=24&Year=2020&lng=en

Additional information:
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Sundial Grower Top Leaf Strawberry Cannabis [Canada]

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Sundial Grower Top Leaf Strawberry Cream Dried Cannabis Pre-Rolls Recall [Canada]

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Canada/Ottawa: Sundial Growers Inc., a Calgary, Alberta establishment, recalls an estimated 30,576 units (one batch/lot) of Sundial Grower branded Top Leaf Strawberry Cream Dried Cannabis Pre-Roll products from the Canadian marketplace due to suspected inaccurate THC labeling and consequential excessive drug potency, both serious health and safety hazards.

HCSC: http://ht.ly/4I7J30qBiPX

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/72877r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Sundial Grower branded Dried Cannabis products are subject to this recall:

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Apotex APO-Metformin Diabetes Medication Recall [Canada]

Canada FlagCanada/Ottawa: Logo - Apotex Inc.Apotex Inc., a Toronto, Ontario establishment, recalls certain batch/lots of the APO-Metformin ER Diabetes medication from the Canadian marketplace due to levels of Nitrosamines (“NDMA”) in excess of Canadian health regulations and consequential long-term risk of certain forms of Cancer, all serious health and safety hazards.

HCSC: http://ht.ly/O6Bt30qfPEy

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/72287a-eng.php

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

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Aurora Cannabis Dried Cannabis Recall [Canada]

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Canada/Ottawa: Logo - Aurora Cannabis Aurora Cannabis Enterprises Ltd., a Cremona, Alberta establishment, recalls an estimated 3060 units (one batch/lot) of Blue Dream Sativa Dried Cannabis due to suspected inaccurate THC labeling and consequential lack of drug potency, both serious health and safety hazards.

HCSC: http://ht.ly/DET930pvxTE

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70865r-eng.php

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

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Zenabis Namaste Wappa Cannabis Recall [Canada]

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Namaste Wappa Dried Cannabis Recall [Canada]

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Canada/Ottawa: Zenabis Ltd., a Vancouver, British Columbia, establishment, recalls an estimated 204 units of Namaste Wappa Dried Cannabis due to suspected mislabelling and consequential risk of incorrect values of THC, all serious health hazards.

HCSC: http://ht.ly/pL0x30p0Bm5

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70271r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Dried Cannabis 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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