Nuri Shogun-X 7000, 69MODE & Thumbs Up 7 Supplements

Nuri Shogun-X 7000, 69MODE Blue 69, Thumbs Up 7 Supplements [US]

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US FlagUS/Silver Spring: Nuri Trading, a Newton, New Jersey, establishment, recalls all current batch/lots of Shogun-X 7000 Supplement Capsules, 69MODE Blue 69 Supplement Capsules, Thumbs Up 7 (Black) 25K Supplement Capsules and Thumbs Up 7 (White) 11K Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs 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/4jiJ30rDJ1l

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nuri-trading-llc-issues-voluntary-nationwide-recall-shogun-x-7000-thumbs-7-black-25k-thumbs-7-white

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

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Ummzy Krazy Night, Shogun-X & Thumbs Up Recall [US]

Ummzy Thumbs Up, Shogun-X & Krazy Night Recall [US]

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US FlagUS/Silver Spring: Ummzy LLC, a Palisades Park, New Jersey establishment, recalls all current batch/lots of Krazy Night Dietary Supplement Capsules, Shogun-X 15000 mg Dietary Supplement Capsules and Thumbs Up 7 Red 70K Dietary Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs 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/TkLw30rDCMy

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ummzy-llc-issues-voluntary-nationwide-recall-thumbs-7-red-70k-shogun-x-15000mg-and-krazy-night-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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BlueSkyGreenEarth AntiBioBotanical & Ly)mex [Australia]

Australia FlagAustralia/Canberra: Logo - The Australian Competition & Consumer Commission ("ACCC")BlueSkyGreenEarth Herbs Pty Ltd., an Alexandria, New South Wales establishment, recalls certain batch/lots of AntiBioBotanical and Ly)mex Herb medications from the Australian marketplace due to suspected Artemisia ingredients and consequential risks of health damage to women of childbearing age and to the health and/or safety of their developing fetus, including reproductive damage, all serious health hazards.

ACCC: http://ht.ly/ewNA30rCFEO

Direct link: https://www.productsafety.gov.au/recall/blueskygreenearth-herbs-pty-ltd-antibiobotanical-and-lymex

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

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Heal the World Hand Sanitizer Recall [US]

Heal the World Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: PNHC, LLC, doing business as Heal the World, a Raleigh, North Carolina establishment, recalls all current batch/lots of Heal the World Hand Sanitizer products sold in 9.6 fluid ounce bottles from the American marketplace due to reported resemblance to water bottles and consequential risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and/or death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/8qzj30rB4kQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pnhc-llc-dba-heal-world-issues-voluntary-nationwide-recall-heal-world-hand-sanitizer-packaged-96

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

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Hilde Hemmes’ Herbals Wormwood Herb Recall [Australia]

Hilde Hemmes' Herbals Wormwood Herb Recall [Australia]

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Australia FlagAustralia/Canberra: Herbal Supplies Pty Ltd, a Ridgehaven, South Australia establishment, recalls certain batch/lots of Hilde Hemmes’ Herbals Wormwood Herb medication from the Australian marketplace due to suspected Artemisia ingredients and consequential risks of health damage to women of childbearing age and to the health and/or safety of their fetus including reproductive damage, all serious health hazards.

ACCC: http://ht.ly/Hrm630rAQ4q

Direct link: https://www.productsafety.gov.au/recall/herbal-supplies-pty-ltd-hilde-hemmes-herbals-wormwood-herb-50g

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

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Bull Wipes All-Purpose Disinfectant Wipe Recall [Canada]

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Canada/Ottawa: Logo - WestCan Health & Safety Ltd.WestCan Health & Safety Ltd., a Coquitlam, British Columbia establishment, recalls all current batch/lots of Bull Wipes All-Purpose Disinfectant Wipes from the Canadian marketplace due to failure to gain Canadian market authorization and risk of possible ineffectiveness and/or microbial contamination, bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/G32r30rAcUh

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75079r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following All-Purpose Disinfectant Wipes are subject to this recall:

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Riva Senna Laxative Tablet Recall [Canada]

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Riva Senna Laxative Tablets Recall [Canada]

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Canada/Ottawa: Laboratoire Riva Inc., a Blainville, Quebec establishment, recalls an estimated two (2) batch/lots of Riva branded Senna Laxative Tablets from the Canadian marketplace due to undisclosed microbial contamination and consequential severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/3Mll30rzWIw

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75089a-eng.php

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

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San Rafael Chemdawg Resin Cannabis Recall [Canada]

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San Rafael Chemdawg Resin Cannabis Recall [Canada]

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Canada/Ottawa: Aurora Cannabis Enterprises Ltd., a Cremona, Alberta establishment, recalls an estimated 19,716 units of San Rafael ’71 OG Chemdawg Live Resin Cannabis products from the Canadian marketplace due to failure to properly label the internal package with consequential risks of overdose, liver and/or kidney damage and other life-changing injuries, all serious health and safety hazards.

HCSC: http://ht.ly/Nq9c30rzF0z

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75047r-eng.php

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

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We Grow BC Dried Cannabis Recall [Canada]

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We Grow BC Dried Cannabis Recall [Canada]

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Canada/Ottawa: We Grow BC Ltd., a Calgary, Alberta establishment, recalls one batch/lot (an estimated 1,980 units) of We Grow BC Ltd.’s Qwest Pineapple Cake Dried Cannabis Pre-Roll products from the Canadian marketplace due to reported incorrect packaging with an inaccurate THC value and consequential risks of THC impairment, decreased ability to operate machines, disorientation and injury, all serious health and safety hazards.

HCSC: http://ht.ly/pCeC30ry9PP

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75023r-eng.php

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

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Gloria Herbs Liver Detox Recall [Australia]

Gloria Herbs Liver Detox Recall [Australia]

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Australia FlagAustralia/Canberra: Gloria Herbs Pty Ltd, a Sydney, New South Wales establishment, recalls certain batch/lots of Dr. Benny Fan’s Series Gloria Herbs branded Liver Detox medication from the Australian marketplace due to suspected Artemisia ingredients and consequential risks of damage to women of childbearing age and to the health and/or safety of their fetus including reproductive damage, all serious health hazards.

ACCC: http://ht.ly/CLRt30ry0uU

Direct link: https://www.productsafety.gov.au/recall/gloria-herbs-pty-ltd-gloria-herbs-liver-detox

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

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Mexican Hand Sanitizer Import Alert [US]

US FlagUS/Silver Spring: Logo - The US Food and Drug Administration ("FDA")The US Food and Drug Administration (“FDA”), a Silver Spring, Maryland-based statutory regulatory and food safety authority, places all Alcohol-based Hand Sanitizers manufactured in Mexico on a countrywide Import Alert to help stop products that appear to be in violation from entering the United States until the FDA is able to review the products’ safety.

This Import Alert was initiated due to a sharp increase in Hand Sanitizer products manufactured in  Mexico that were labeled to contain Ethanol (also known as Ethyl Alcohol) as an active agent but instead tested positive for Methanol contamination. Methanol, or Wood Alcohol, is an industrial-use substance that can be toxic when absorbed through the skin and life-threatening when ingested and can result in Nausea, Vomiting, Headache, Blurred Vision, Permanent Blindness, Seizures, Coma, permanent damage to the Nervous System and/or Death.

FDA: http://ht.ly/nBuU30ruMK9

Direct link: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-takes-action-place-all-alcohol-based-hand-sanitizers-mexico-import

Additional information:
The US Food and Drug Administration (“FDA”) reports its analyses of Alcohol-based Hand Sanitizers imported from Mexico found eighty-four percent (84%) of the samples analyzed by the agency from April through December 2020 were not in compliance with the FDA’s safety regulations, as follows:

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Life Basics by Nourished Life Sunscreen Recall [Australia]

Life Basics by Nourished Life Sunscreen Recall [Australia]

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Australia FlagAustralia/Canberra: BWX Digital Pty Ltd., a Dandenong, South Victoria establishment, recalls certain batch/lots of Life Basics by Nourished Life branded SPF30 Natural Coconut Body Sunscreen from the Australian marketplace due to suspected failure to homogenize medicinal ingredients and consequential risks of sun protection failure, burns and serious skin damage, all serious health hazards.

ACCC: http://ht.ly/SHdA30ruEnf

Direct link: https://www.productsafety.gov.au/recall/bwx-digital-pty-ltd-life-basics-by-nourished-life-spf30-natural-coconut-body-sunscreen

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

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Apple iPhone 12 Interference Warning [US]

Apple iPhone 12 Implantable Device Warning

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US FlagUS/Cupertino: Apple Inc., a Cupertino, California establishment, warns Apple iPhone 12 owners and users to keep their phones at least six (6) inches / fifteen (15) cm away from any implantable device such as pacemakers and/or defibrillators due to possible electronic interference, damage and/or operational failure to life-supporting equipment.

Apple: http://ht.ly/DrX230ruBNp

Direct link: https://support.apple.com/en-us/HT211900

Additional information:
Apple reports magnets and radios inside iPhone devices and MagSafe accessories could cause interference with certain medical devices, as follows:

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Scalpa Numb Anesthetic Cream Recall [US]

Scalpa Numb Anesthetic Cream Recall [US]

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US FlagUS/Washington: Scalpa Inc., a Phoenix, Arizona establishment, recalls an estimated 10,000 tubes of Scalpa Numb Maximum Strength Topical Anesthetic Cream 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/Jf6430rt21h

Direct link: https://www.cpsc.gov/Recalls/2021/Scalpa-Recalls-Scalpa-Numb-Maximum-Strength-Topical-Anesthetic-Cream-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Scalpa Numb Maximum Strength Topical Anesthetic Cream marketed, sold and delivered in the United States, as follows:

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Infants’ Friend Oral Liquid Medication Recall [Australia]

Australia FlagInfants' Friend Oral Liquid Medication Recall [Australia]Australia/Canberra: Infants’ Friend Pty Ltd., an Ipswich, Queensland establishment, recalls certain batch/lots of Infants’ Friend Oral Liquid from the Australian marketplace due to suspected Chloroform contamination and consequential risks of liver damage, kidney damage and nervous system damage, all serious health hazards.

ACCC: http://ht.ly/yvNN30rtehc

Direct link: https://www.productsafety.gov.au/recall/infants-friend-pty-ltd-infants-friend-oral-liquid-100ml

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

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