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

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

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US FlagUS/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):

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Food Recall: King’s Hawaiian Pretzel Products

Food Recall: King’s Hawaiian Pretzel Products

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US FlagUS/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:

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

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

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US FlagUS/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):

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Drug Recall: Vi-Jon Magnesium Citrate Saline Laxatives

Vi-Jon Magnesium Citrate Saline Laxative Recall [US]

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US FlagUS/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):

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

Food  Recall: Aloha, Glucerna, Imperial, Lyons, MRE & Pirq Beverages

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US FlagUS/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):

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Drug Recall: Ultra Supplement Launch Sequence Capsules

Drug Recall: Ultra Supplement Launch Sequence Supplements

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US FlagCanada FlagUS/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:

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Drug Recall: Sustango Nutritional Supplement Capsules

Drug Recall: Sustango Nutritional Supplement Capsules

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US FlagUS/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:

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Drug Recall: Aivia Whey Protein Meal Replacement

Aivia Whey Protein & Power Herbs Meal Replacement Supplement Recall [US]

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US FlagUS/Silver Spring: Nature’s Sunshine Products Inc., a Spanish Fork, Utah establishment, recalls certain batch/lots of Aivia Whey Protein & Power Herbs Meal Replacement Supplement products from the American marketplace due to suspected mislabeling and consequential undeclared Milk, a known allergen, source of dietary intolerance 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.

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

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natures-sunshine-products-inc-issues-allergy-alert-undeclared-milk-aivia-whey-protein-power-herbs

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

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Drug Recall: Natreve Vegan Protein Supplement Powder

Drug Safety: Natreve Vegan Protein Supplement Powder [US]

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US FlagUS/Silver Spring: Natreve, a Vancouver, British Columbia establishment, recalls certain batch/lots of Vegan Protein Supplement Powder products from the American marketplace due to suspected mislabeling and consequential undeclared Milk, a known allergen, source of dietary intolerance 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.

FDA: https://bit.ly/3IdTvV2

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natreve-issues-voluntary-recall-limited-us-batches-natreve-vegan-protein-powder-french-vanilla-wafer

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

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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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Drug Recall: Best Naturals Organic Wintergreen Essential Oil

Best Naturals Organic Wintergreen Essential Oil [US]

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US FlagUS/Washington: Best Nutritionals LLC, a Piscataway, New Jersey establishment, recalls an estimated 2,800 Best Naturals Organic Wintergreen Essential Oils 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/kKlF30sjnkR

Direct link: https://www.cpsc.gov/Recalls/2022/Best-Nutritionals-Recalls-Organic-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Organic Wintergreen Essential Oil products, as follows:

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NaturesPlus Keto Living Sugar Control Supplements [US]

NaturesPlus Keto Living Sugar Control Capsule Supplements Recall [US]

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US FlagUS/Silver Spring: Natural Organics, Inc., an Amityville, New Yoek establishment, recalls certain batch/lots of NaturesPlus Keto Living Sugar Control Capsule Supplements from the American marketplace due to suspected suspected mislabeling and consequential undeclared Gluten, a known allergen, source of dietary intolerance 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.

FDA: http://ht.ly/1bCg30sjcpO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natural-organics-inc-issues-nationwide-voluntary-recall-four-lots-naturesplus-keto-living-sugar

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

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Rae Prenatal Capsules & Rae Immunity Supplements [US]

Rae Prenatal Capsules & Rae Immunity Capsules [US]

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US FlagUS/Bethesda: Rae Wellness, a Minneapolis, Minnesota establishment, recalls an estimated 191,200 Rae Prenatal Capsules and Rae Immunity Capsules 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/Mbns30shmsM

Direct link: https://www.cpsc.gov/Recalls/2022/Rae-Wellness-Recalls-Prenatal-and-Immunity-Dietary-Supplements-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves Rae Nutritional Supplement products, as follows:

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Pink Pussycat 3000 Dietary Supplements [US]

Pink Pussycat 3000 Dietary Supplements [US]

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US FlagUS/Silver Spring: F&S Medical Supply, doing business as Pink Toyz, a Chatsworth, California establishment, recalls certain batch/lots of Pink Pussycat 3000 Dietary Supplements from the American marketplace due to undeclared Sildenafil, 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 requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/zQoh30sgI64

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fs-medical-supply-dba-pink-toyz-issues-voluntary-nationwide-recall-pink-pussycat-capsules-due

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

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Havyco Vy & Dietary Supplement Teas [Australia]:

Havyco Vy & Tea

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Australia FlagAustralia/Canberra: Vy & Tea Australia, a Melbourne, Victoria establishment, recalls certain batch/lots of Havyco Vy & Tea products from the Australian marketplace due to undeclared Phenolphthalein and Sibutramine with consequential elevated risks of cardiac events as well as increased risks of certain types of Cancers, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

ACCC: http://ht.ly/83b030sfJnW

Direct link: https://www.productsafety.gov.au/recalls/vy-tea-australia-%E2%80%94-havyco-vy-tea-45g

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Dietary Supplement Tea products are subject to this recall:

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