Abba Medix Sage N Sour Dried Cannabis Recall [Canada]

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Abba Medix Sage N Sour Dried Cannabis Recall [Canada]

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Canada/Ottawa: Abba Medix Corp., a Pickering, Ontario establishment, recalls an estimated 72 units of Sage N Sour Dried Cannabis products from the Canadian marketplace due to reported failure to properly identify the active cannabinoid values for THC and Total THC in a single batch/lot of the medication and consequential risks of THC impairment, decreased ability to operate machines and disorientation, all serious health and safety hazards.

HCSC: http://ht.ly/cakO30rfQz6

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/74027r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Dried Cannabis products are subject to this recall:

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Lidl Cologran Sucralose Sweetener Recall [UK]

Lidl Cologran Sucralose Sweetener Recall [UK]

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UK FlagUK/London: Lidl Great Britain Limited (“Lidl GB”), a London, England establishment and subsidiary of Lidl of Stiftung & Co KG of Neckarsulm, Baden-Wüttenberg, Germany, recalls a certain batch/lot of Cologran Sucralose Sweetener Tablets from the British marketplace due to undeclared Aspartame (also known as E951). This artificial sweetener is made with the chemical Phenylalanine poses as serious health and safety hazards for people with Phenylketonuria (also called “PKU”) as well as people taking certain medications for their mental health.

FSA: http://ht.ly/QuSj30rfbNB

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-47-2020

Additional information:
The UK Food Standards Agency (“FSA”) reports the following chemical Sweetener products are subject to recall:

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Organic Aromas Wintergreen Essential Oil Recall [US]

13631 - CPSC - Organic Aromas Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Organic Aromas LLC, a Boise, Idaho establishment, recalls an estimated 300 Organic Aromas Wintergreen Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/ow1Q30rf0XR

Direct link: https://www.cpsc.gov/Recalls/2020/Organic-Aromas-Recalls-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Organic Aromas Wintergreen Essential Oil products sold and delivered in amber glass bottles with white or black caps, as follows:

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Lidl Cologran Stevia Sweetener Recall Update [UK]

Lidl Cologran Stevia Sweetener Tablet Recall [UK]

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UK FlagUK/London: Lidl Great Britain Limited (“Lidl GB”), a London, England establishment and subsidiary of Lidl of Stiftung & Co KG of Neckarsulm, Baden-Wüttenberg, Germany, updates its existing recall for a single batch/lot of Cologran Stevia Sweetener Tablets, a Stevia variant, from the British marketplace to include additional batch/lots.

The original recall was initiated due to undeclared Aspartame (also known as E951), an artificial sweetener made with the chemical Phenylalanine and consequential possible Carcinogenic risks as well as serious health and safety hazards for people with Phenylketonuria (also called “PKU”) as well as people taking certain medications for their mental health.

FSA: http://ht.ly/Q5sc30reuRc

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-45-2020-update-1

Additional information:
The UK Food Standards Agency (“FSA”) reports the following chemical Sweetener products are subject to recall:

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Lidl Cologran Stevia Sweetener Recall [UK]

Lidl Cologran Stevia Sweetener Tablet Recall [UK]

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UK FlagUK/London: Lidl Great Britain Limited (“Lidl GB”), a London, England establishment and subsidiary of Lidl of Stiftung & Co KG of Neckarsulm, Baden-Wüttenberg, Germany, recalls certain batch/lots of Cologran Stevia Sweetener Tablets, a Stevia variant, from the British marketplace due to undeclared Aspartame (also known as E951), an artificial sweetener made with the chemical Phenylalanine and consequential possible Carcinogenic risks as well as serious health and safety hazards for people with Phenylketonuria (also called “PKU”) as well as people taking certain medications for their mental health.

FSA: http://ht.ly/GvaK30rcpbw

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-45-2020

Additional information:
The UK Food Standards Agency (“FSA”) reports the following chemical Sweetener products are subject to recall:

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Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

Vitamin Shoppe Vthrive Bioactive Multivitamin Recall [US]

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US FlagUS/Washington: The Vitamin Shoppe, a Secaucus, New Jersey establishment, recalls an estimated 8,200 bottles of Vthrive Bioactive Multivitamins from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/X2WJ30rcqVr

Direct link: https://www.cpsc.gov/Recalls/2020/The-Vitamin-Shoppe-Recalls-Vthrive-Bioactive-Multivitamins-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Multivitamins, as follows:

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Medi-First, Medique, Dover, Otis Clapp & Ecolab Med Recall

Medi-First, Medique, Dover, Otis Clapp & Ecolab Med Recall

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US FlagUS/Washington: Medique, a Fort Myers, Florida establishment, recalls an estimated 143,300 Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp and Ecolab branded medications and/or health products from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/aPaY30r9OOg

Direct link: https://www.cpsc.gov/Recalls/2020/Medique-Recalls-31-Different-Over-the-Counter-Drugs-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Sold-Exclusively-on-Amazon-com-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports the recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp and Ecolab, as follows (in alphabetical order):

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Red-E Male Enhancement Supplement Recall [US]

Red-E Male Enhancement Supplement Recall [US]

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US FlagUS/Silver Spring: The Protein Shoppe, LLC, a Pharr, Texas establishment, recalls certain batch/lots of Red-E Male Enhancement Tablet products from the American marketplace due to suspected undeclared Sildenafil, an FDA approved drug for the treatment of Male Erectile Dysfunction in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors and consequential risk of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/hLfX30r80lE

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/protein-shoppe-llc-issues-voluntary-nationwide-recall-red-e-male-enhancement-tablet-due-presence

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

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Simplers Botanicals Wintergreen Essential Oil Recall [US]

Simplers Botanicals Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Nutraceutical Corporation, a Park City, Utah establishment, recalls an estimated 14,000 bottles of Simplers Botanicals branded Organic Wintergreen (Gaultheria Fragrantissiam) Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/Go2i30r4Rjh

Direct link: https://www.cpsc.gov/Recalls/2020/Nutraceutical-Recalls-Simplers-Botanicals-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Organic Wintergreen Essential Oils, as follows:

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BioCeuticals Vitamin D3 Liquid Drops Recall [Australia]

Australia FlagAustralia/Canberra: Logo - FIT-BioCeuticals LimitedFIT-BioCeuticals Limited, a Surry Hills, New South Wales establishment, recalls certain batch/lots of BioCeuticals Vitamin D3 Drops Forte Liquid products from the Australian marketplace due to suspected incomplete medication mixing and consequential non-uniform consistency, strength and texture throughout the batch/lot with risks of medication over-dose, under-dose and/or premature spoilage, all serious health hazards.

ACCC: http://ht.ly/tNwZ30r4kL3

Direct link: https://www.productsafety.gov.au/recall/fit-bioceuticals-limited-bioceuticals-vitamin-d3-drops-forte-liquid-20ml

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

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Nature’s Oil Wintergreen & Birch Essential Oil Recall [US]

Nature’s Oil Wintergreen and Birch Essential Oil Recall ]US]

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US FlagUS/Washington: Bulk Apothecary, an Aurora, Ohio establishment, recalls an estimated 20,240 bottles of Nature’s Oil Wintergreen and Birch Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/i2xU30r3gRL

Direct link: https://www.cpsc.gov/Recalls/2020/Bulk-Apothecary-Recalls-Natures-Oil-Wintergreen-and-Birch-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Nature’s Oil Wintergreen and Birch Essential Oils, as follows:

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Taro-Dermovate & Taro-Clobetasol Cream Recall [Canada]

Canada FlagCanada/Ottawa: Logo - Taro Pharmaceuticals IncTaro Pharmaceuticals Inc, a Brampton, Ontario establishment and subsidiary of Taro Pharmaceutical Industries Ltd. of Haifa, Israel recalls certain batch/lots of Taro-Dermovate Cream and Taro-Clobetasol Cream USP from the Canadian marketplace due to suspected product mixing irregularities and consequential risk of failure to meet content uniformity standards with possible under- and/or over-dose administration, all serious health and safety hazards.

HCSC: http://ht.ly/myJ930r1o7K

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73615r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Drugs are subject to this recall:

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Ferring DDAVP Drug Spray Recall [Canada]

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Ferring DDAVP Drug Spray Recall [Canada]

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Canada/Ottawa: Ferring Pharmaceuticals Inc., a Toronto, Ontario establishment, recalls certain batch/lots of DDAVP Spray (Desmopressin Acetate Nasal solution, 10 micrograms/spray) because the product may contain a higher than labelled dose of the active ingredient (Desmopressin), a consequential risk of drug overdose, a serious health hazard.

HCSC: http://ht.ly/jYQ030r07uq

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73567a-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Desmopressin Acetate Prescription Drug products are subject to this recall:

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Ferring DDAVP Drug Spray Recall [Canada]

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Ferring DDAVP Drug Spray Recall [Canada]

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Canada/Ottawa: Ferring Pharmaceuticals Inc., a Toronto, Ontario establishment, recalls certain batch/lots of DDAVP Spray (Desmopressin Acetate Nasal solution, 10 micrograms/spray) because the product may contain a higher than labelled dose of the active ingredient (Desmopressin), a consequential risk of drug overdose, a serious health hazard.

HCSC: http://ht.ly/4KXF30qZhLh

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73575r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Prescription Drug products are subject to this recall:

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Pranarom Wintergreen Essential Oil Recall [US]

Pranarom Wintergreen Essential Oil Recall [US]

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US FlagUS/Washington: Pranarom, a Minneapolis, Minnesota establishment, recalls an estimated 960 bottles of Pranarom branded Wintergreen Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/cHWX30qYq0I

Direct link: https://www.cpsc.gov/Recalls/2020/Pranarom-Recalls-Wintergreen-Essential-Oils-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain bottles of Wintergreen Essential Oil products, as follows:

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