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:

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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Ausganica Soothing Herbs Toothpaste Recall [Australia]

Australia FlagAustralia/Canberra: Ausganica Soothing Herbs Toothpaste Recall [Australia]Trueway International recalls certain batch/lots of Ausganica Soothing Herbs Toothpaste due to suspected Comfrey, a banned ingredient under Australian legislation and a serious health hazard. ACCC: http://ht.ly/r78H30f8Pbq

Direct link: https://www.productsafety.gov.au/recall/trueway-international-ausganica-soothing-herbs-toothpaste

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

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Garden of Life Baby Organic Supplement Recall [US]

US FlagUS/Silver Spring: Garden of Life Baby Organic Liquid Recall [US]Garden of Life, LLC recalls certain batch/lots of Dr. Formulated brand Baby Organic Liquid Supplement due to possible misinterpretation of administration instructions and consequential risk of difficulties in swallowing and resultant choking hazard. FDA: http://ht.ly/s6MI30f1abA

Direct link: https://www.fda.gov/Safety/Recalls/ucm575135.htm

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

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Bella Pharmaceuticals Sterile Drug Recall [US]

US FlagUS/Silver Spring: Bella Pharmaceuticals Sterile Drug Recall [US]Bella Pharmaceuticals, Inc. recalls all batch/lots of its Sterile Drug Products due to suspected lack of Sterility Assurance, a serious and potential fatal situation, requiring immediate medical intervention. FDA: http://ht.ly/eZug30eLbOo

Direct link: https://www.fda.gov/Safety/Recalls/ucm572373.htm

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

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