Plant Therapy branded Essential Oil Recall [US]

Plant Therapy branded Essential Oil Recall [US]

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US FlagUS/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:

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EU issues 51 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 13/2020 of its Rapid Alert System containing fifty one (51) consumer, automotive 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/6DP430qt7OL

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=14&Year=2020&lng=en

Additional information:
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EU issues 43 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 12/2020 of its Rapid Alert System containing forty three (43) consumer, automotive 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/WB0B30qrH35

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=13&Year=2020&lng=en

Additional information:
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Active Male Dietary Supplement Recall [US]

Active Male Dietary Supplement Recall [US]

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US FlagUS/Silver Spring: Natural Remedy Store, a San Antonio, Texas establishment, recalls all current batch/lots of Active Male Dietary Supplement Capsules due to suspected undeclared Tadalafil, an existing FDA approved drug for certain medical conditions and legally available only under prescription from a licensed physician. The undeclared presence of this medication can pose a serious health and safety hazard for some people.

FDA: http://ht.ly/W7RA30qrMHX

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natural-remedy-store-issues-voluntary-worldwide-recall-active-male-due-presence-undeclared-tadalafil

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

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EU issues 41 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 11/2020 of its Rapid Alert System containing forty one (41) consumer, automotive 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/Thf830qq6o1

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=12&Year=2020&lng=en

Additional information:
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EU issues 38 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 10/2020 of its Rapid Alert System containing 38 (thirty eight) consumer, automotive 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/Mmpt30qohNM

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=11&Year=2020&lng=en

Additional information:
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American Health Ranitidine Tablet Recall [US]

American Health Ranitidine Tablet Recall [US]

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US FlagUS/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:

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