Drug Recall: Loud Muscle Launch Sequence Supplements

Drug Recall: Loud Muscle Launch Sequence Supplements

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US FlagCanada FlagUS/Silver Spring: Loud Muscle Science, LLC, a Hauppauge, New York establishment, recalls certain batch/lots of Launch Sequence Supplement Capsules from the American and Canadian marketplaces due to reported undeclared Tadalafil, an FDA approved drug for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: https://bit.ly/3NzIvSY

Direct US link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/loud-muscle-science-llc-issues-voluntary-recall-launch-sequence-capsules-due-presence-undeclared

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

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Mylan Pharmaceuticals Insulin Glargine [US]

US FlagUS/Silver Spring: Logo - Mylan Pharmaceuticals IncMylan Pharmaceuticals Inc., a Pittsburgh, Pennsylvania establishment, has recalled one (1) batch/lot of its Insulin Glargine (Insulin glargine- yfgn) Injection, 100 units/mL (U-100), packaged in 10 mL vials from the United States marketplace due to reported mislabeling, as follows:

Additional information:
According to the company, this drug product is not the branded Semglee vial but, in fact, the unbranded Insulin Glargine- yfgn. This batch is being recalled due to the potential for the label to be missing on some vials. The product information, batch number and expiry date information are present on the carton.

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Clearchoice Foam Face Shields [Canada]

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Clearchoice Foam Face Shields Recall [Canada]

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Canada/Ottawa: Southmedic, a Barrie, Ontario establishment, recalls certain batch/lots of Clearchoice Foam Face Shields from the Canadian marketplace due to mislabeling and consequential undeclared Latex, a known allergen, source of skin and/or respiratory intolerance and/or sensitivity, and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

HCSC: http://ht.ly/9jAt30setbI

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/clearchoice-foam-face-shields

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Personal Protective Equipment (“PPE”) products are subject to this recall:

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Bioderma Sensibio H20 Micellar Water Makeup Remover

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Bioderma Sensibio H20 Micellar Water Makeup Remover Recall [Canada]

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Canada/Ottawa: NAOS Canada Inc., a Pierreville, Québec establishment, recalls an estimated 6,270 Bioderma Sensibio H20 Micellar Water Makeup Remover products from the Canadian marketplace due to suspected Serratia marcescens bacterial contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

HCSC: http://ht.ly/4YiT30scOG1

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/bioderma-sensibio-h2o-micellar-water-makeup-remover-recalled-due-microbial

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

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Drug Recall: Rise Up Red Edition Dietary Supplements

Rise Up Red Edition Capsule Dietary Supplements [US]

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US FlagUS/Silver Spring: Positive-Health, a Wilmington, Delaware establishment, recalls certain batch/lots of Rise Up Red Edition Capsule Dietary Supplements from the American marketplace due to reported undeclared Tadalafil, an FDA approved drug for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/yuHA30sbffQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/positive-health-issues-voluntary-nationwide-recall-rise-red-edition-capsules-due-presence-undeclared

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

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Hard Dawn Rise and Shine Supplements [US]

Hard Dawn Rise and Shine Supplements [US]

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US FlagUS/Silver Spring: Esupplementsales, LLC, an Orangevale, California establishment, recalls certain batch/lots of Hard Dawn Rise and Shine Dietary Supplements from the American marketplace due to reported undeclared Tadalafil, an FDA approved drug for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/WZJC30s9z9x

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/esupplementsales-llc-issues-nationwide-recall-one-lot-hard-dawn-due-presence-undeclared-tadalafil

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

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Equate Dry Mouth Oral Rinse Mouthwash [Canada]

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Equate Dry Mouth Oral Rinse Mouthwash Recall [Canada]

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Canada/Ottawa: The Shandex Sales Group, a Pickering, Ontario establishment, recalls an estimated 468 bottles of Equate branded Dry Mouth Oral Rinse Mouthwash products from the Canadian marketplace due to suspected Klebsiella pneumonia bacterial contamination and consequential risks of Gram-negative bacterial infection, healthcare-associated infections (“HAIs”), including Pneumonia, bloodstream infections, wound or surgical site infections and/or other life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

HCSC: http://ht.ly/3ZJL30s6sg2

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/equate-dry-mouth-oral-rinse-recalled-due-microbial-contamination

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

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Genius Kids & Teens Health Supplement Recall [Canada]

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Genius Kids and Teens Natural Health Dietary Supplements Recall [Canada]

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Canada/Ottawa: Nutripur Inc., a Boisbriand, Quebec establishment, recalls one (1) known batch/lot of Genius Kids and Teens Natural Health Dietary Supplements from the Canadian marketplace due to suspected Staphylococcus aureus contamination and consequential risks of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

HCSC: http://ht.ly/hGDA30rWMaj

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76593a-eng.php

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

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Bayer Tinactin Powder Spray Recall [Canada]

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Bayer Tinactin Powder Spray Recall [Canada]

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Canada/Ottawa: Bayer Inc., a Mississauga, Ontario establishment, recalls certain batch/lots of Tinactin branded Chill Deodorant Powder Spray, Tinactin branded Aerosol Powder and Tinactin branded Chill Liquid Spray from the Canadian marketplace due to suspected Benzene contamination and consequential risks of Cancers of the Blood and Blood-Forming Tissues, including the Bone Marrow and the Lymphatic System including Leukemia, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

HCSC: http://ht.ly/81XR30rWzEo

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76575r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Tinactin Chill Deodorant Powder Spray products are subject to this recall:

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GSK Advil Cold & Sinus Day/Night Drug Recall [Canada]

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GSK Advil Cold & Sinus Day/Night Drugs Recall [Canada]

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Canada/Ottawa: GlaxoSmithKline Consumer Healthcare ULC (“GSK”), a Mississauga, Ontario establishment, recalls certain batch/lots of Advil Cold & Sinus Day/Night Convenience Packs from the Canadian marketplace due to suspected mispackaging and/or mislabeling and consequential risks of incorrect dosing, inability to reliably operate machinery, falls, laceration, concussion, bone fractures and/or central nervous system (“CNS”) injury, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.

HCSC: http://ht.ly/RZm330rW4dS

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76571a-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Advil Cold & Sinus medications are subject to this recall:

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Pfizer Chantix (Varenicline) Tablet Recall [US]

Pfizer Chantix Tablet Recall [US]

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US FlagUS/Silver Spring: Pfizer, a Manhattan, New York establishment, recalls certain batch/lots of Chantix Tablets due to the presence of N-nitroso-varenicline contamination and consequential risks of increased carcinogenicity (Cancer), severe illness and/or possible life-changing complications, all serious health and safety hazards/situations requiring immediate medical intervention to minimize suffering and prevent life-changing injury.

FDA: http://ht.ly/sDqw30rRBS6

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-expands-voluntary-nationwide-recall-include-four-additional-lots-chantixr-varenicline-tablets

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

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Applaws, AVA & by Sainsbury’s Cat Food Recall Update [UK]

Applaws, AVA and by Sainsbury’s Cat Food Recall [UK]

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UK FlagUK/London: Fold Hill Foods, a Boston, Lincolnshire, England establishment, updates its existing recall for certain batch/lots of Applaws, AVA and by Sainsbury’s Cat Food products from the British marketplace to include all best-before dates for Applaws products with the site code GB218E5009.

The original recall notification was initiated due to suspected Pancytopenia infection and consequential risks of Anemia (low levels of red blood cells), Leukopenia (low levels of white blood cells and/or Thrombocytopenia (low platelet levels), all serious health and safety situations requiring immediate veterinary intervention.

FSA: http://ht.ly/7qMp30rN5Iq

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-36-2021-update-1

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

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Applaws, AVA & by Sainsbury’s Cat Food Recall [UK]

Applaws, AVA and by Sainsbury’s Cat Food Recall [UK]

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UK FlagUK/London: Fold Hill Foods, a Boston, Lincolnshire, England establishment, recalls certain batch/lots of Applaws, AVA and by Sainsbury’s Cat Food products from the British marketplace due to suspected Pancytopenia infection and consequential risks of Anemia (low levels of red blood cells), Leukopenia (low levels of white blood cells and/or Thrombocytopenia (low platelet levels), all serious health and safety situations requiring immediate veterinary intervention.

FSA: http://ht.ly/LSHr30rMcXX

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-36-2021

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

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LifeSeasons Blood Nourish-R Supplement Recall [US]

LifeSeasons Blood Nourish-R Supplement Recall [US]

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US FlagUS/Washington: LifeSeasons Inc., a Springville, Utah establishment, recalls an estimated 7,800 bottles of LifeSeasons Blood Nourish-R Supplements 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/I2l030rLH8e

Direct link: https://www.cpsc.gov/Recalls/2021/UST-Recalls-Bottles-of-LifeSeasons-Blood-Nourish-R-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain LifeSeasons Blood Nourish-R Supplements marketed, sold and delivered in the United States, as follows:

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Puricia Hand Sanitizer Recall [Canada]

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Puricia Hand Sanitizer Recall [Canada]

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Canada/Ottawa: Pharmaberg Inc., a Delta, British Columbia establishment, recalls certain batch/lots of Puricia Hand Sanitizer products from the Canadian marketplace due to reported undeclared impurities as well as Benzene and Methanol contamination at elevated levels with consequential risks of operational ineffectiveness, failure to prevent microbial spread and possible bacterial and/or viral contamination, all serious health and safety hazards.

HCSC: http://ht.ly/cOx430rLD7t

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75845r-eng.php

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

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