Product Recall: Tootsie Baby Teethers & Teether Key Toys

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Canada/Ottawa: CTG Brands Inc., a Vaughan, Ontario establishment, recalls an estimated 9,901 Tootsie Baby branded Water-Filled Teethers and Teether Keys Children’s Toys from the Canadian marketplace due to suspected Bacillus cereus and Omithinibacillus californiensis bacterial contamination as well as Candida parapsilosis yeast contamination with consequential risks of Gram-positive bacterial infection and/or fungal infection, severe illness and/or possible life-changing complications, 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: https://bit.ly/3PXhnOO

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/tootsie-baby-water-filled-teethers-and-teether-keys-recalled-due-microbial

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

Food Recall: Aloha, Glucerna, Imperial, Lyons & Pirq Drinks

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US/Silver Spring: Lyons Magnus LLC (“Lyons Magnus”), a Fresno, California establishment, expands its existing recall for certain batch/lots of Aloha, Glucerna, Imperial, Kate Farms, Lyons, MRE, Oatly, Pirq, Premier Protein and Stumptown branded Nutritional or Medicinal Beverage products from the American marketplace to include additional products, best-by dates and/or batch/lot codes.

The original recall was initiated due to the potential for microbial contamination, including Cronobacter Sakazakii, with 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.

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

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lyons-magnus-expands-voluntary-recall-include-additional-nutritional-and-beverage-products-due

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

Food Recall: King’s Hawaiian Pretzel Products

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US/Silver Spring: King’s Hawaiian, a Los Angeles establishment, recalls certain batch/lots of its King’s Hawaiian branded Pretzel Slider Buns, Pretzel Hamburger Buns and Pretzel Bites products from the American marketplace due to the potential for microbial contamination, including Cronobacter Sakazakii, with 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.

FDA: https://bit.ly/3w1rxqL

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kings-hawaiianr-issues-voluntary-recall-pretzel-slider-buns-pretzel-hamburger-buns-and-pretzel-bites

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

Food Recall: Aloha, Glucerna, Imperial, Lyons & Pirq Drinks

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US/Silver Spring: Lyons Magnus LLC (“Lyons Magnus”), a Fresno, California establishment, expands its existing recall for certain batch/lots of Aloha, Glucerna, Imperial, Kate Farms, Lyons, MRE, Oatly, Pirq, Premier Protein and Stumptown branded Nutritional or Medicinal Beverage products from the American marketplace to include additional products, best-by dates and/or batch/lot codes.

The original recall was initiated due to the potential for microbial contamination, including Cronobacter Sakazakii, with 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.

FDA: https://bit.ly/3zSbBZ2

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lyons-magnus-expands-voluntary-recall-include-additional-nutritional-and-beverage-products-due

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

Drug Recall: Vi-Jon Magnesium Citrate Saline Laxatives

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US/Silver Spring: Vi-Jon, LLC, a Smyrna, Tennessee establishment, recalls certain batch/lots of all current batch/lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor from the American marketplace due to suspected Gluconacetobacter liquefaciens 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.

FDA: https://bit.ly/3djuf4t

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vi-jon-llc-expands-voluntary-nationwide-recall-magnesium-citrate-saline-laxative-oral-solution-lemon

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

Food Recall: Aloha, Glucerna, Imperial, Lyons & Pirq Drinks

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US/Silver Spring: Lyons Magnus LLC (“Lyons Magnus”, a Fresno, California establishment, recalls certain batch/lots of Aloha, Glucerna, Imperial, Kate Farms, Lyons, MRE, Oatly, Pirq, Premier Protein and Stumptown branded Nutritional or Medicinal Beverage products from the American marketplace due to the potential for microbial contamination, including Cronobacter Sakazakii, with 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.

FDA: https://bit.ly/3A0F9Vr

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lyons-magnus-voluntarily-recalls-53-nutritional-and-beverage-products-due-potential-microbial

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

Drug Recall: Ultra Supplement Launch Sequence Capsules

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US/Silver Spring: Ultra Supplement LLC., a Wilmington, Delaware establishment, recalls certain batch/lots of Launch Sequence Aphrodisia and Euphoria Supplement Capsules 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:  https://bit.ly/3SblDwC

Direct 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:

Drug Recall: Sustango Nutritional Supplement Capsules

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US/Silver Spring: Ultra Supplement LLC, a Wilmington, Delaware establishment, recalls certain batch/lots of Sustango Nutritional Supplement Capsules 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: https://bit.ly/3Bviy4y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ultra-supplement-llc-issues-voluntary-nationwide-recall-sustango-due-presence-undeclared-tadalafil

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

Food Recall: Encore Beef Dog Food

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UK/London: Encore recalls certain batch/lots of Encore Beef Selection Dog Food products from the British marketplace due to suspected metal fragment contamination and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and sepsis, all serious health and safety hazards requiring immediate veterinary intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FSA: https://bit.ly/3OFTgDG

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-44-2022

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

Drug Recall: Loud Muscle Launch Sequence Supplements

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US/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:

Mylan Pharmaceuticals Insulin Glargine [US]

US/Silver Spring: Mylan 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.

Product Recall: Clearchoice Foam Face Shields

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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:

Bioderma Sensibio H20 Micellar Water Makeup Remover

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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:

Drug Recall: Rise Up Red Edition Dietary Supplements

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US/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:

Hard Dawn Rise and Shine Supplements [US]

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US/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: