Abba Medix Sage N Sour Dried Cannabis Recall [Canada]

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Canada/Ottawa: Abba Medix Corp., a Pickering, Ontario establishment, recalls an estimated 72 units of Sage N Sour Dried Cannabis products from the Canadian marketplace due to reported failure to properly identify the active cannabinoid values for THC and Total THC in a single batch/lot of the medication and consequential risks of THC impairment, decreased ability to operate machines and disorientation, all serious health and safety hazards.

HCSC: http://ht.ly/cakO30rfQz6

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/74027r-eng.php

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

Omnigon Hydroframe Medical Device Recall [Australia]

Australia/Canberra: Omnigon Pty Ltd, a Burnley, Victoria establishment, recalls certain batch/lots of Hydroframe Stoma Medical Devices from the Australian marketplace due to undeclared Manuka Honey, a known allergen, source of sensitisation and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

ACCC: http://ht.ly/eRSD30rfCR7

Direct link: https://www.productsafety.gov.au/recall/omnigon-pty-ltd-hydroframe-with-manuka-honey

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

Barbie, Hot Wheels & PAW Patrol Hand Sanitizer Recall [US]

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US/Silver Spring: Ashtel Studios, an Ontario, California establishment, recalls certain batch/lots of Children’s Character Licensed Hand Sanitizer products from the American marketplace due to reported resemblance to Children’s Food or Drink Containers and consequential risks of child poisoning, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/cG2y30rd7KO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ashtel-studios-issues-voluntary-recall-licensed-hand-sanitizers-packaged-084-fluid-ounce-pouches-due

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

DMM VISSION Cleaner branded Hand Sanitizer Recall [US]

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US/Silver Spring: DMM VISSION SA de CV, an Estado de México, México establishment, recalls at least five (5) batch/lots of Cleaner branded Hand Sanitizer from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/XsbW30rcQ9x

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dmm-vission-sa-de-cv-issues-voluntary-nationwide-recall-cleaner-hand-sanitizer-500-ml-and-1200-ml

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

EU issues 30 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 39/2020 of its Rapid Alert System containing thirty (30) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/7ho230rbDSI

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000013&Year=2020&lng=en

Additional information:

Aerowipe Cleansing Wipe Recall [Australia]

Australia/Canberra: Aero Healthcare, an Armidale, New South Wales establishment, recalls certain batch/lots of Aerowipe Cleansing Wipes supplied in various First Aid Kits from the Australian marketplace due to suspected mould contamination and consequential risks of infection, sepsis and severe illness and/or possible life-changing complications, all serious health hazards.

ACCC: http://ht.ly/ZsTV30rc4PO

Direct link: https://www.productsafety.gov.au/recall/aero-healthcare-aerowipe-cleansing-wipes-supplied-in-various-first-aid-kits

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

EU issues 26 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 38/2020 of its Rapid Alert System containing twenty-six (26) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/ukBu30rarFB

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000012&Year=2020&lng=en

Additional information:

M branded Hand Sanitizer Alcohol Antiseptic Recall [US]

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US/Silver Spring: Medek, LLC, an Alamo, Texas establishment, recalls all current batch/lots of M branded Hand Sanitizer Alcohol Antiseptic 80% from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/cBfc30raJ7f

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medek-llc-issues-voluntary-nationwide-recall-m-hand-sanitizer-due-potential-presence-methanol-wood

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

EU issues 25 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 37/2020 of its Rapid Alert System containing twenty-five (25) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/kmYH30r9yIG

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000011&Year=2020&lng=en

Additional information:

BD Alaris Infusion Pump System Recall [US]

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US/Silver Spring: Becton, Dickinson and Company (“BDC”), a Franklin Lakes, New Jersey establishment, updates its existing recall for various models of BD Alaris Infusion Pump Systems from the American marketplace after an upgrading and reclassification of the original notification published by the US Food and Drug Administration (“FDA”) to Class I, the most serious and potentially deadly classification of medical device recall.

The original recall was initiated due to possible operational failure and consequential inaccurate dosage, failure to dose and possible life-changing complications including death, all serious health and safety hazards.

FDA: http://ht.ly/Irmt30r8C9r

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-provides-update-previously-disclosed-recall-bd-alaris-system-hardware

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

EU issues 23 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 36/2020 of its Rapid Alert System containing twenty-three (23) consumer, automotive, commercial and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/ged030r8kOO

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000010&Year=2020&lng=en

Additional information:

Leafree Instant Hand Sanitizer Recall [US]

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US/Silver Spring: CorgioMed, LLC, a Gaithersburg, Maryland establishment, recalls all current batch/lots of Leafree Instant Hand Sanitizer-Aloe Vera from the American marketplace due to reported labelling as “EDIBLE ALCOHOL” and consequential risks of inadvertent alcohol poisoning, alcohol toxicity and GI tract laceration damage, all serious health and safety hazards.

FDA: http://ht.ly/466S30r8mCQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/corgiomed-llc-issues-voluntary-nationwide-recall-all-lots-leafree-instant-hand-sanitizer-aloe-vera

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

bio aaa Advance Hand Sanitizer Recall [US]

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US/Silver Spring: AJR Trading LLC, a Tlalnepantia, Mexico establishment, recalls an estimated 2,004 units of bio aaa branded Advance Hand Sanitizer from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/JHhL30r8hJo

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ajr-trading-llc-issues-voluntary-nationwide-recall-bio-aaa-advance-hand-sanitizer-480-ml-bottles-lot

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

Always Be Clean & Just Hand branded Sanitizer Recall [US]

US/Silver Spring: Open Book Extracts (“OBX”), a Roxboro, North Carolina establishment, recalls certain batch/lots of Always Be Clean Hand Sanitizer and Just Hand Sanitizer products from the American marketplace labeled to contain Methanol (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/TqQU30r7NED

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/open-book-extracts-issues-voluntary-nationwide-recall-all-lots-always-be-clean-hand-sanitizer-and

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

Harmonic Nature Topical Solution Sanitizer Gel Recall [US]

US/Silver Spring: Harmonic Nature, a Guadalupe, Nuevo Leon Mexico establishment, recalls all 800 bottles of Harmonic Nature branded Topical Solution Hand Sanitizer Gel from the American marketplace due to suspected 1-Propanol contamination and consequential risks of GI tract burns, central nervous system depression, permanent CNS impairment and/or death, all serious health and safety hazards.

FDA: http://ht.ly/uDN230r7xqE

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/harmonic-nature-issues-voluntary-nationwide-recall-hand-sanitizer-due-presence-1-propanol

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