Tweed LBS Ocean View Dried Cannabis Recall [Canada]

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Canada/Ottawa: Tweed Dried Cannabis Recall [Canada]Tweed, Inc., a Smiths Falls, Ontario establishment, recalls an estimated 1,240 units of LBS Ocean View (Sativa) Dried Cannabis due to suspected mislabeling and consequential incorrect packaging dates with risks of possible drug overdose, all serious health and safety hazards.

HCSC: http://ht.ly/pfNa30oQwMe

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/69924r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves one (1) batch/lot consisting of Tweed Inc.’s branded LBS Ocean View (Sativa) Dried Cannabis sold through authorized provincial or territorial retailers in Ontario and Yukon, as follows:

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Tweed LBS Sunset Dried Cannabis Recall [Canada]

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Canada/Ottawa: Tweed Dried Cannabis Recall [Canada]Tweed, Inc., a Smiths Falls, Ontario establishment, recalls an estimated 13,575 units of LBS Sunset (Indica) Dried Cannabis due to suspected mislabeling and consequential incorrect Cannabinoid values with risks of overdose, all serious health and safety hazards.

HCSC: http://ht.ly/y8Zm30o3CFJ

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/69256r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves one (1) batch/lot consisting of Tweed branded LBS Sunset (Indica) Dried Cannabis sold through authorized provincial and territorial retailers in British Columbia, Alberta, Saskatchewan, Manitoba, Ontario, Quebec, New Brunswick, Nova Scotia, Newfoundland, Prince Edward Island, Northwest Territories and Nunavut, as follows:

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Aurora Cannabis Recall [Canada]

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Canada/Ottawa: Logo - Aurora CannabisAurora Cannabis Enterprise Inc., a Cremona, Alberta establishment, recalls an estimated two batch/lots consisting of an estimated 2,180 units of Aurora Cannabis products due to suspected mislabeling and consequential inclusion of a different Cannabis product with potential for over dosage, all potential serious health and safety hazards.

HCSC: http://ht.ly/HZlu30nApyr

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/68982r-eng.php

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

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CannTrust Liiv Cannabis Oil Recall [Canada]

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Canada/Ottawa: Logo - CannTrustCannTrust, a Vaughan, Ontario establishment, recalls batch/lot F344 of CannTrust Liiv Cannabis Oil due to suspected mislabeling and consequential inclusion of a different Cannabis product with potential for over dosage, all potential serious health and safety hazards.

HCSC: http://ht.ly/ktdH30nyj9I

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/68938r-eng.php

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

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Up Cannabis Inc. Eldo Dried Cannabis Recall [Canada]

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Canada/Ottawa: Logo - Up Cannabis Inc.Up Cannabis Inc., an Oakville, Ontario establishment, recalls an estimated 1,428 units of Up Cannabis Eldo Dried Cannabis due to suspected mould (mold) contamination and consequential risk of respiratory irritation and/or infection, severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/Sx5A30nie5w

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/68798r-eng.php

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

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Medex Supply CoaguChek XS Test Strip Recall [US]

US FlagUS/Silver Spring: Medex Supply CoaguChek XS Test Strip Recall [US]Terrific Care, LLC. doing business as Medex Supply Distribution Inc., a Passaic, New Jersey establishment, recalls certain batch/lots of CoaguChek XS Test Strips due to suspected risk of inaccurately high INR test results and consequential risk of initiating inappropriate therapeutic measures such as Warfarin dose reduction, interruption of Warfarin medication use or inappropriate administration of Vitamin K, all serious health and safety hazards.

FDA: http://ht.ly/KLq330ncX4Y

Direct link: https://www.fda.gov/Safety/Recalls/ucm628976.htm

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

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Results RNA Lubrisine Eye Drop Recall [US]

US FlagUS/Silver Spring: Results RNA Lubrisine Eye Drop Recall [US]Results RNA LLC, a New Hartford, Connecticut establishment, recalls all current batch/lots of Lubrisine Eye Drops to the nationwide/worldwide healthcare practitioner, retail and consumer levels due to suspected production using practices that do not support sterility as well as undeclared Colloidal Silver and consequential risk of bacterial infection, severe illness and/or possible life-changing complications including long-term eye damage, visual impairment and/or blindness, all serious health hazards.

FDA: http://ht.ly/j8az30nc18j

Direct link: https://www.fda.gov/Safety/Recalls/ucm629256.htm

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

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