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):

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:

Drug Recall: Aivia Whey Protein Meal Replacement

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US/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:

Drug Recall: Natreve Vegan Protein Supplement Powder

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US/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:

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:

NaturesPlus Keto Living Sugar Control Supplements [US]

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US/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:

Pink Pussycat 3000 Dietary Supplements [US]

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US/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:

Reckitt Airborne Fruit Flavor Supplement Gummies [US]

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US/Bethesda: RB Health (US) LLC, doing business as Reckitt, a Parsippany, New Jersey establishment, recalls an estimated 3.74 million bottles of Reckitt Airborne Assorted Fruit Flavor Supplement Gummies from the American marketplace due to suspected packaging overpressure and consequential risks of eye injury and laceration upon sudden bottle decompression, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury.

CPSC: http://ht.ly/4s2330seym2

Direct link: https://www.cpsc.gov/Recalls/2022/Reckitt-Recalls-More-than-Three-Million-Bottles-of-Airborne-Gummies-Due-to-Injury-Hazard

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Airborne Supplement Gummies marketed, sold and delivered in the United States, as follows:

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:

Moor Herbs Angel Infant Formula [US]

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US/Silver Spring: Moor Herbs, a Detroit, Michigan establishment, recalls all batch/lots of Moor Herbs Angel Infant Formula from the American marketplace due to reported meet specific nutrition and labeling requirements for infant formula. In addition, when the product was tested, the Iron, Sodium, and Potassium content were well over the maximum allowed, which could potentially lead to Iron overload and/or Electrolyte imbalances. In addition, the product did not have Vitamin D, and a Vitamin D deficiency can potentially lead to Rickets, a softening and weakening of bones, 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/xKxe30s6Pku

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/moor-herbs-recalls-angel-formula-infant-formula-because-possible-health-risk

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