Drug Recall: Dr. Rima Recommends Nano Silver Supplements

Click to enlarge

US/Silver Spring: Natural Solutions Foundation, a Newton, New Jersey establishment, recalls certain batch/lots of Dr. Rima Recommends Nano Silver Dietary Supplements from the American marketplace due to suspected unsubstantiated health claims that the product will prevent, treat, or cure COVID-19, claims that the FDA says may prevent patients who use this product from seeking timely medical treatment run the risk of serious, life-threatening health consequences, 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/3mTIBNr

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-notice-product-recall

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

Drug Recall: Sandoz Aprepitant Caps, Lidocaine/Prilocaine Cream

Click to enlarge

US/Washington: Sandoz Inc., a Princeton, New Jersey establishment, recalls an estimated 156,750 Aprepitant Capsules and Lidocaine/Prilocaine Cream from the American marketplace due to 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: https://bit.ly/423xRw3

Direct link: https://www.cpsc.gov/Recalls/2023/Sandoz-Recalls-Aprepitant-Capsules-and-Lidocaine-and-Prilocaine-Cream-Prescription-Drugs-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 Aprepitant Capsules and Lidocaine and Prilocaine Cream products marketed, sold and delivered in the United States, as follows:

Drug Recall: Boots Kids Daily Health Multivitamin Gummies

Click to enlarge

UK/London: Boots UK Limited, a Nottingham, England establishment, recalls certain batch/lots of Boots branded Kids Daily Health Multivitamins Strawberry Flavour Gummies from the British marketplace due to suspected mislabeling and/or mispackaging with consequential undeclared Soya (Soy), 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.

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

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-aa-11-2023

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

Drug Recall: EzriCare & Delsam Pharma Eye Drops

Click to enlarge

US/Silver Spring: Global Pharma Healthcare, a Chennai, Tamilnadu, India establishment, recalls all current batch/lots of EzriCare and Delsam Pharma branded Artificial Tears Lubricant Eye Drops from the American marketplace due to suspected Verona Integron-mediated Metallo-β-lactamase (VIM)- and Guiana-Extended Spectrum-β-Lactamase (GES)-producing carbapenem-resistant Pseudomonas aeruginosa (VIM-GES-CRPA) contamination with consequential risks of eye infections, permanent loss of vision and bloodstream infection, 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/3XjZJZk

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-pharma-healthcare-issues-voluntary-nationwide-recall-artificial-tears-lubricant-eye-drops-due

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

Health Advisory: EzriCare Artificial Tears

Click to enlarge

US/Atlanta: The US Centers for Disease Control and Prevention (“CDC”), an Atlanta, Georgia based health promotion and disease prevention authority, issues a Health Advisory against the use of certain batch/lots of EzriCare Artificial Tears due to suspected multi-state infections with an extensively drug-resistant strain of Verona Integron-mediated Metallo-β-lactamase (“VIM”) and Guiana-Extended Spectrum-β-Lactamase (“GES”)-producing Carbapenem-resistant Pseudomonas Aeruginosa (VIM-GES-CRPA) and consequential risks of bacterial infection, severe illness and/or possible life-changing complications including visual impairment and/or blindness, all serious and potential fatal hazards, requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CDC: https://bit.ly/3Y3p6Qg

Direct link: https://emergency.cdc.gov/han/2023/han00485.asp?ACSTrackingID=USCDC_511-DM98842&ACSTrackingLabel=HAN%20485%20-%20General%20Public&deliveryName=USCDC_511-DM98842

Additional information:
The US Centers for Disease Control and Prevention (“CDC”) reports the following Drugs are subject to this Health Advisory:

Drug Recall: Weed Me Cannabis Extract

Click to enlarge

Canada/Ottawa: Weed Me Inc., a Pickering, Ontario establishment, recalls an estimated 1230 units of Diamond District Sativa Pre-Rolls Cannabis Extract from the Canadian marketplace due to incorrect Cannabinoid values, where the THC and total THC labelled is higher than the actual THC and total THC and consequential risks of lack of medicinal potency, failure to manage pain and failure to provide neurological symptom relief, 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: https://bit.ly/3WMWOsW

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/weed-me-inc-recalls-one-lot-diamond-district-sativa-pre-rolls-cannabis-extract

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

Drug Recall: Vicks VapoRub Xtra Strong Vaporizing Ointment

Click to enlarge

Australia/Canberra: Procter & Gamble Australia Pty. Limited, a Macquarie Park, New South Wales establishment, recalls certain batch/lots of Vicks VapoRub Xtra Strong Vaporizing Ointment from the Australian marketplace due to suspected mispackaging and consequential risks of overdose, allergic reactions including rash, blistering, hives, skin peeling, itching and/or swelling. In addition, steam inhalation by children aged 6 to 10 may result in an increased risk of adverse events such as ocular irritation, headaches, dizziness, nausea and cardiac stress in the form of Tachycardia, 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: https://bit.ly/3PSL6u8

Direct link: https://www.productsafety.gov.au/recalls/procter-gamble-australia-pty-ltd-%E2%80%94-vicks-vaporub-xtra-strong-100g

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following topical drugs to relieve Cough and Cold symptoms are subject to this recall:

Drug Recall: Power Life Nutrition High Impact Plant Protein

Click to enlarge

Canada/Ottawa: Power Life Nutrition, a Woodland Hills, California establishment, recalls certain batch/lots of High Impact Plant Protein Chocolate Flavor Supplements from the Canadian 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.

CFIA: https://bit.ly/3BNt9Hj

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/power-life-tony-horton-brand-high-impact-plant-protein-chocolate-flavor-recalled-due

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Protein Supplement products are subject to this recall:

Drug Recall: Power Life Nutrition High Impact Plant Protein

Click to enlarge

US/Silver Spring: Power Life Nutrition, a Woodland Hills, California establishment, recalls certain batch/lots of High Impact Plant Protein Supplements from the American marketplace due to suspected mislabeling and/or mispackaging 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/3PBLgpw

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/thgh-partners-llc-issues-allergy-alert-undeclared-milk-power-life-plant-protein

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

Drug Recall: Holland & Barrett Soya Lecithin Supplements

Click to enlarge

UK/London: Holland & Barrett, a Nuneaton, Warwickshire establishment, recalls certain batch/lots of Holland & Barrett branded Soya Lecithin Soft Gel Supplement Capsules from the British marketplace due to suspected mislabeling and consequential undeclared Peanuts, 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.

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

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-aa-61-2022

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

Drug Recall: Bed Head, Dove, Suave & TRESemmé Shampoo

Click to enlarge

US/Silver Spring: Unilever United States, a Englewood Cliffs, New Jersey establishment, recalls certain batch/lots of Unilever’s Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head) and TRESemmé branded Dry Shampoo Aerosol products from the American marketplace due to suspected elevated levels of Benzene 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-altering injury or death.

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

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/unilever-issues-voluntary-us-recall-select-dry-shampoos-due-potential-presence-benzene

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

Drug Recall: Aivia Whey Protein Meal Replacement

Click to enlarge

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

Click to enlarge

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:

NaturesPlus Keto Living Sugar Control Supplements [US]

Click to enlarge

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:

Havyco Vy & Dietary Supplement Teas [Australia]:

Click to enlarge

Australia/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: