Plant Therapy branded Essential Oil Recall [US]

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US/Washington: Plant Therapy LLC, a Twin Falls, Idaho establishment, recalls an estimated 34,000 Plant Therapy branded Wintergreen Essential Oils and Essential Oil Blends with Wintergreen products from the American marketplace due to suspected failure to meet the child resistant packaging requirements specified by the Poison Prevention Packaging Act (“PPPA”) and consequential risks of choking, poisoning and GI tract laceration damage, all serious safety hazards.

CPSC: http://ht.ly/lX5K30quext

Direct link: https://www.cpsc.gov/Recalls/2020/Plant-Therapy-Recalls-Wintergreen-Essential-Oils-and-Essential-Oil-Blends-with-Wintergreen-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain 1/3 fluid ounce (approximately 10 mL), 1 fluid ounce (30 mL) and 3.3 fluid ounce (100 mL) amber glass bottles with black caps of Plant Therapy Wintergreen (“Gaultheria procumbens”), Organic Wintergreen (“Gaultheria procumbens”), Muscle Aid Synergy Blend (undiluted), Tingly Mint Synergy Blend and Vein Aid Synergy Blend (undiluted) products sold prior to September 20, 2019, as follows:

American Health Ranitidine Tablet Recall [US]

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US/Silver Spring: American Health Packaging, a Columbus, Ohio establishment, recalls eleven (11) lots of Ranitidine Tablets, USP 150 mg, 100 count Unit Dose Blisters from the American marketplace due to suspected levels of N-Nitrosodimethylamine (“NDMA”), a probable Human Carcinogen, above the allowable limits established by the FDA and consequential risk of Cancer, all serious health hazards.

FDA: http://ht.ly/gFcQ30qnOVO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-health-packaging-issues-voluntary-nationwide-recall-ranitidine-tablets-usp-150-mg-100-count

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

Inogen One G3 Oxygen Concentrator Recall [Australia]

Australia/Canberra: Air Liquide Healthcare Pty Ltd, a Melbourne, Victoria establishment, recalls certain batch/lots of Inogen One G3 Concentrator Portable Lightweight Medical Oxygen Machines from the Australian marketplace due to suspected operational failure and consequential risk of oxygen supply loss, asphyxiation and death, all serious health and safety hazards.

ACCC: http://ht.ly/tq9D30qmtPY

Direct link: https://www.productsafety.gov.au/recall/air-liquide-healthcare-pty-ltd-inogen-one-g3-concentrator

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

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: