Pur Naturals brand Bone Broth Protein Recall [Canada]

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Pur Naturals brand Bone Broth Protein Recall [Canada]

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Canada/Ottawa: Pur-Natural Ingredients of Canada recalls certain batch/lots of Pur Naturals brand Bone Broth Protein products due to undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

CFIA: http://ht.ly/zvyj30o6gzR

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/inspection/2019/69346r-eng.php

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Bone Broth Protein products are subject to this recall:

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Sunstone Organics Kratom Supplement Recall [US]

US FlagUS/Silver Spring: Logo - US Food and Drug AdministrationSunstone Organics, an Eugene, Oregon establishment, recalls certain batch/lots of Sunstone Organics branded Maeng Da Kratom and Sunstone Organics branded White Vein Kratom Supplements due to suspected risk of Salmonella contamination and consequential risk of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/TIGE30nVXu3

Direct link: https://www.fda.gov/Safety/Recalls/ucm632554.htm

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

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Rhino 5k Dietary Supplement Recall [US]

US FlagUS/Silver Spring: Rhino 5k Dietary Supplement Recall [US]Happy Together, Inc. a Boynton Beach, Florida, establishment, recalls all current batch/lots of Rhino 5k Dietary Supplement Capsules due to suspected Sildenafil and Tadalafil contamination, all serious health and safety hazards.

FDA: http://ht.ly/JBPm30nfyPo

Direct link: https://www.fda.gov/Safety/Recalls/ucm629353.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement 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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GNC Women’s Iron Dietary Supplement Recall [US]

US FlagUS/Washington: GNC Women's Iron Dietary Supplement Recall [US]General Nutrition Corp., a Pittsburgh, Pennsylvania establishment recalls an estimated 756,000 blister packs of GNC Women’s Iron Complete Dietary Supplement products due to suspected failure to meet US Federal child resistant closure requirements and consequential risk of ingestion, poisoning, kidney damage and overdose, all serious health hazards.

CPSC: http://ht.ly/qlaZ30n5Dqs

Direct link: https://www.cpsc.gov/Recalls/2019/Womens-Iron-Complete-Supplements-Recalled-by-GNC-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain GNC branded Women’s Iron Complete Dietary Supplements, sold in 60-count caplets.

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Zero Xtreme branded Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: Zero Xtreme branded Nutritional Supplement Recall [US]Zero Xtreme, a Marathon, Florida establishment, recalls certain batch/lots of Zero Xtreme branded Nutritional Supplement Capsules due to suspected presence of Sibutramine, a controlled substance under FDA regulation that was marketed as an appetite suppressant but withdrawn from the US market in 2010 due to suspected increased risks of Cardiovascular Events and Stroke, all serious health and safety hazards.

FDA: http://ht.ly/InAy30mgeRW

Direct link: https://www.fda.gov/Safety/Recalls/ucm623503.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following over-the-counter (“OTC”) drugs are subject to this recall:

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Abbott Two Cal & Promote Diet Supplement Recall [Canada]

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Canada/Ottawa: Abbott Two Cal & Promote Diet Supplement Recall [Canada]Abbott Nutrition, a Saint-Laurent, Québec establishment, recalls certain batch/lots of Abbott Two Cal brand and Abbott Promote brand Formulated Liquid Diet products due to suspected risk of unspecified bacterial contamination and consequential risk of bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

CFIA: http://ht.ly/QFeb30m8dt7

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/inspection/2018/67800r-eng.php

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Formulated Liquid Diet products are subject to this recall:

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