MyNicNaxs Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: MyNicNaxs Nutritional Supplement Recall [US]MyNicNaxs, LLC, a Deltona, Florida establishment, has recalled all lots of various Dietary Supplements due to suspected presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil, all controlled substances and undeclared active pharmaceutical ingredients (“APIs”). The presence of Diclofenac, Phenolphthalein, Sibutramine and/or Sildenafil in the recalled Dietary Supplements renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. Due to their ingredients, these Supplements all pose serious health and safety hazards. FDA: http://ht.ly/zYCx30kVBsI

Direct link: https://www.fda.gov/Safety/Recalls/ucm613197.htm

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

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Sandoz & Novartis Drug Blister Package Recall [US]

US FlagUS/Washington: Sandoz and Novartis Drug Blister Package Recall [US]Sandoz and Novartis recall an estimated 470,000 Prescription Drug Blister Packages due to suspected failure to meet child-resistant closure requirements as required by the US Poison Prevention Packaging Act and consequential risk of choking, ingestion and poisoning, all serious health and safety hazards.

CPSC: http://ht.ly/qXyk30kR2SM

Direct link: https://www.cpsc.gov/Recalls/2018/Sandoz-and-Novartis-Recall-Prescription-Drug-Blister-Packages-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirements

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Blister Packages of various Prescription Drugs branded by Novartis and Sandoz. The Drugs are packaged with three (3) to ten (10) tablets per blister card.

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Blissful Remedies branded Kratom Powder Recall [US]

US FlagUS/Silver Spring: Blissful Remedies branded Kratom Powder Recall [US]Blissful Remedies, a Las, Vegas establishment, recalls certain batch/lots of Red Maeng Da, Gold Series Ultra Enhanced Indo and Kratom+CBD., CBD Maeng Da infused Kratom Powder Supplement products, due to suspected 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/kYYi30kOVr6

Direct link: https://www.fda.gov/Safety/Recalls/ucm612376.htm

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

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Gaia Ethnobotanical Kratom Supplement Recall [US]

US FlagUS/Silver Spring: Logo - Gaia EthnobotanicalGaia Ethnobotanical, LLC, a Los Vegas, Nevada establishment, recalls certain batch/lots of Kratom Products due to suspected Salmonella contamination and consequential risk of gram-negative bacterial infection and illness, all serious health hazards.

FDA: http://ht.ly/us5030kDeCI

Direct link: https://www.fda.gov/Safety/Recalls/ucm611438.htm

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

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Jamp-Glucose Supplement Recall [Canada]

Canada FlagCanada/Ottawa: Jamp Pharma branded Jamp-Glucose Supplement Recall [Canada]Jamp Pharma Corporation, a Boucherville, Quebec establishment, has recalled three (3) batch/lots of Jamp-Glucose 50 and three (3) lots of Jamp-Glucose 75 D-glucose Supplements due to insufficient levels of D-glucose and consequential risk of false negative Oral Glucose Challenge or Tolerance Test results and failure to correctly screen and diagnosis Diabetes, all serious health hazards.

HCSC: http://ht.ly/2FJ630kyXWj

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67008a-eng.php

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

The affected lots have been recalled because the level of D-glucose they contain is up to nearly five times lower than what is declared on the label, as follows:

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Medline Cosmetic Product Recall [Canada]

Canada Flag

Canada/Ottawa: Medline Cosmetic Product Recall [Canada]Medline Canada, Corp. a Milton, Ontario establishment, recalls an estimated 44,000 Medline Cosmetic products due to suspected Burkolderia cepacia contamination and consequential risk of gram negative bacterial infection and illness, all serious health hazards.

HCSC: http://ht.ly/t02k30kqnFF

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66910r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves various Medline Remedy Cosmetic products as identified below. The affected products are sold in white packaging with batch/lot numbers printed on the bottom of each dispensing bottle as follows (in alphabetical order):

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Apotex Fluticasone Propionate Nasal Spray Recall [US]

US FlagUS/Silver Spring: Apotex Fluticasone Propionate Nasal Spray Recall [US]Apotex Corp., a Toronto, Ontario establishment, recalls certain batch/lots of Fluticasone Propionate Nasal Spray, USP, due to suspected glass fragment contamination and consequential risk of spray blockage, oral and/or nasal injury, and respiratory tract laceration damage, all serious health and safety hazards.

FDA: http://ht.ly/WA1N30knb4I

Direct link: https://www.fda.gov/Safety/Recalls/ucm609436.htm

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

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