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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Splish Splash Gentle Baby Wash Recall [US]

US FlagUS/Silver Spring: Splish Splash Gentle Baby Wash Recall [US]Saje Natural Wellness, a Malibu, California establishment, recalls certain batch/lots of Splish Splash Gentle Baby Wash products due to suspected Pseudomonas aeruginosa 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/KY6B30kQB1I

Direct link: https://www.fda.gov/Safety/Recalls/ucm612744.htm

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

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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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Perceval Sutureless Heart Valve Warning [Canada]

Canada FlagCanada/Ottawa: Perceval Sutureless Heart Valve Warning [Canada]LivaNova Canada Corp., a Burnaby, British Columbia establishment, issues warning concerning an unknown number of Perceval Sutureless Heart Valves due to “stent folding” and consequential risks of operational failure and need for surgical re-operation, all serious health and safety hazards.

HCSC: http://ht.ly/YSvY30kNvvC

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67146r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Heart Valves are subject to this warning notification:

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Paragon branded Oxygenator Recall [Canada]

Canada FlagCanada/Ottawa: Logo - Health CanadaChalice Medical Limited, a Worksop, Nottinghamshire, UK establishment, recalls certain Paragon branded Oxygenators due to suspected wrong expiry dates and consequential risk of operational impairment and possible injury, all serious health and safety hazards.

HCSC: http://ht.ly/2uYH30kFB7j

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67094r-eng.php

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

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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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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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