Magic Mobility Power Wheelchair Recall [Australia]

Australia/Canberra: Red Milawa Pty Ltd trading as Magic Mobility, a Noble Park, Victoria establishment, recalls certain batch/lots of Magic Mobility Power Wheelchairs due to suspected structural failure and consequential risk of back support rotation or collapse to horizontal and patient injury, all serious safety hazards.

ACCC: http://ht.ly/ivyS30pOBK4

Direct link: https://www.productsafety.gov.au/recall/red-milawa-pty-ltd-t-as-magic-mobility-magic-mobility-power-wheelchair

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

Convex Two-Piece Skin Barrier Recall [Australia]

Australia/Canberra: ConvaTec Australia Pty Ltd, a Victoria, New South Wales establishment, recalls certain batch/lots of various Convex Two-Piece Skin Barriers due to suspected device centering failure and consequential risk of laceration damage, all serious health and safety hazards.

ACCC: http://ht.ly/3d5930pxXZT

Direct link: https://www.productsafety.gov.au/recall/convatec-australia-pty-ltd-various-convex-two-piece-skin-barriers

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

Aurora Cannabis Dried Cannabis Recall [Canada]

Canada/Ottawa: 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:

Major Pharmaceuticals Milk of Magnesia Recall [US]

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US/Silver Spring: Plastikon Healthcare, LLC, a Lawrence, Kansas establishment, recalls certain batch/lots of Major Pharmaceuticals branded Milk of Magnesia 2400 mg/30 mL Oral Osmotic Laxative products, due to suspected risk of high levels of unspecified aerobic bacterial contamination and consequential risk of bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/1TJq30pvqkQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/plastikon-healthcare-issues-voluntary-nationwide-recall-milk-magnesia-oral-suspension-2400-mg30-ml

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

Jimy Long Reach Lift Trolley Jack Recall [Australia]

Australia/Canberra: Jimy Industrial Pty Ltd, a Dudley Park, South Australia establishment, recalls certain batch/lots of Long Reach Super Low Profile Quick Lift Trolley Jack due to suspected failure to labelling the product for applicable warnings and dangers and consequential risk of collapse under weight, laceration, fractures, crush and death, all serious safety hazards.

ACCC: http://ht.ly/gEeE30pu87z

Direct link: https://www.productsafety.gov.au/recall/jimy-industrial-pty-ltd-long-reach-super-low-profile-quick-lift-trolley-jack-1800kg

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

Sandoz Losartan Potassium & Ezetimibe Drug Recall [US]

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US/Washington: Sandoz Inc., a Princeton, New Jersey establishment, recalls an estimated 636,000 Losartan Potassium Prescription Drug and Ezetimibe Prescription Drug Bottles due to suspected failure to meet child-resistant closure requirements as required by the US Poison Prevention Packaging Act and consequential risk of choking, ingestion and poisoning, all serious health and safety hazards.

CPSC: http://ht.ly/2wC230proqE

Direct link: https://www.cpsc.gov/Recalls/2019/Sandoz-Recalls-Losartan-Potassium-and-Ezetimibe-Prescription-Drug-Bottles-Due-to-Failure-to-Meet-ChildResistant-Closure-Requirements

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Bottles of prescription medications Losartan Potassium and Ezetimibe from Sandoz with certain identified batch/lot numbers.

Hollister Urostomy Bag Recall [Australia]

Australia/Canberra: Liberty Medical Pty Ltd, a Box Hill, Victoria establishment, recalls certain batch/lots of Hollister branded Urostomy Bags due to suspected film failure and consequential risk of local site injury and bacterial infection, all serious health and safety hazards.

ACCC: http://ht.ly/nefX30plhUo

Direct link: https://www.productsafety.gov.au/recall/liberty-medical-pty-ltd-hollister-urostomy-bag

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