Aurora Cannabis Medical Marijuana Recall [Canada]

Canada FlagCanada/Ottawa: Health Canada LogoAurora Cannabis Enterprises Inc. recalls certain batch/lots of Sundance Borealis blend (Sativa) Dried Marijuana due to formulation and/or packaging errors and consequential potency inconsistencies, a serious health hazard. HCSC: http://ht.ly/oITd30gE5sj

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/65110r-eng.php

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

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Baxter International Nexterone Injection Recall [US]

US FlagUS/Silver Spring: Baxter International Nexterone Injection Recall [US]Baxter International Inc. recalls certain batch/lots of Nexterone (Amiodarone HCl) 150 mg/100 mL Premixed Injection due to suspected particulate contamination and consequential risk of vein irritation, inflammatory reaction, aggravation of preexisting infections, allergic reactions, phlebitis, pulmonary emboli, pulmonary granulomas, immune system dysfunction, pulmonary dysfunction, pulmonary infarction and systemic embolization, all serious health and safety hazards. FDA: http://ht.ly/DUlX30gBAhx

Direct link: https://www.fda.gov/Safety/Recalls/ucm585155.htm

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

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Apo-Perindopril Arginine Recall [Australia]

Australia FlagAustralia/Canberra: Apo-Perindopril Arginine Recall [Australia]Apotex Pty Ltd. recalls certain batch/lots of Apo-Perindopril Arginine drugs used to treat High Blood Pressure, Heart Failure or Coronary Artery Disease due to suspected silica contamination, a possible health and safety hazard. ACCC: http://ht.ly/VtdG30gAr8e

Direct link: https://www.productsafety.gov.au/recall/apotex-pty-ltd-apo-perindopril-arginine-25-mg-5-mg-and-10-mg-tablets-bottle

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Drugs are subject to this recall:

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Pfizer Australia Gentamicin Recall [Australia]

Australia FlagAustralia/Canberra: Pfizer Australia GentamicinPfizer Australia Pty Ltd. recalls certain batch/lots of Gentamicin Injection BP 80 mg due to suspected higher than expected amounts of Histamine, a serious health hazard. ACCC: http://ht.ly/m1ak30fLlIh

Direct link: https://www.productsafety.gov.au/recall/pfizer-australia-pty-ltd-gentamicin-injection-bp-80-mg-in-2-ml-steriluer-ampoules-in-packs-of-10-or-50

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Pfizer Australia Gentamicin are subject to this recall:

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Paediatric Leuprorelin Acetate Recall [Australia]

Australia FlagAustralia/Canberra: Paediatric Leuprorelin Acetate Recall [Australia]AbbVie Pty Ltd. recalls certain batch/lots of Lucrin Depot Paediatric Leuprorelin Acetate due to suspected insufficient mixing and consequential risk of incomplete delivery of medication, a serious health hazard. ACCC: http://ht.ly/xm5R30fCKOn

Direct link: https://www.productsafety.gov.au/recall/abbvie-pty-ltd-lucrin-depot-paediatric-leuprorelin-acetate-30mg-for-injection-prefilled-dual-chamber-syringe-single-dose

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

Vegetable Vigra Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: Vegetable Vigra brand Nutritional Supplement Recall [US]Natures Supplement, Inc. recalls an estimated 260 bottles of Vegetable Vigra brand Nutritional Supplements due to suspected undeclared Sildenafil an FDA approved drug for the treatment of Erectile Dysfunction, all serious health and safety hazards. FDA: http://ht.ly/N6YG30fnc98

Direct link: https://www.fda.gov/Safety/Recalls/ucm576834.htm

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

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AFT Pharma brand Lax Sachet Recall [Australia]

Australia FlagAustralia/Canberra: Australian Competition & Consumer CommissionAFT Pharmaceuticals Pty Ltd recalls certain batch/lots of Lax Sachets due to suspected incorrect dosage/administration instructions and consequential risk of reduced effectiveness of the product, a serious health hazard. ACCC: http://ht.ly/mKll30flgjE

Direct link: https://www.productsafety.gov.au/recall/aft-pharmaceuticals-pty-ltd-lax-sachets

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

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