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

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

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US FlagUS/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:

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DMM VISSION Cleaner branded Hand Sanitizer Recall [US]

Cleaner branded Hand Sanitizer Recall [US]

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US FlagUS/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:

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M branded Hand Sanitizer Alcohol Antiseptic Recall [US]

M branded Hand Sanitizer Alcohol Antiseptic 80%

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US FlagUS/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:

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Fitting Furniture Bunk Bed Recall [Australia]

Fitting Furniture Bunk Bed Recall [Australia]

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Australia FlagAustralia/Canberra: Fitting Furniture, a Braeside, Victoria establishment, recalls certain batch/lots of Bunk Beds from the Australian marketplace due to suspected component failure and risks of structural failure, collapse, bone fracture, concussion, laceration and death, all serious safety hazards.

ACCC: http://ht.ly/G8oc30r91hW

Direct link: https://www.productsafety.gov.au/recall/fitting-furniture-various-bunk-beds

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

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BD Alaris Infusion Pump System Recall [US]

BD Alaris Infusion Pump System Recall [US]

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US FlagUS/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:

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Leafree Instant Hand Sanitizer Recall [US]

Leafree Instant Hand Sanitizer Recall [US]

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US FlagUS/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:

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bio aaa Advance Hand Sanitizer Recall [US]

bio aaa Advance Hand Sanitizer Recall [US]

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US FlagUS/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:

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

US FlagUS/Silver Spring: Logo - Open Book ExtractsOpen 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:

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Harmonic Nature Topical Solution Sanitizer Gel Recall [US]

US FlagUS/Silver Spring: Logo - US Food and Drug Administration ("FDA")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:

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Zanilast+ Gel Hand Sanitizer Gel Recall [US]

Zanilast+ Gel branded Sanitizer Gel

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US FlagUS/Silver Spring: Nanomateriales, SA de CV, a Monterrey, Mexico establishment, recalls certain batch/lots of Zanilast+ Gel branded 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/sTgH30r7nrp

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nanomateriales-sa-de-cv-issues-voluntary-nationwide-recall-all-lots-zanilastgel-due-presence-1

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

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V-Klean, Medically Minded & Protz Hand Sanitizer Recall [US]

V-Klean, Medically Minded & Protz Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: Asiaticon SA de CV (Mexico), a Mexico City, Mexico establishment, recalls certain batch/lots of V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel and Protz Real Protection Antibacterial Hand Sanitizer products from the American marketplace due to the suspected presence of Methanol (also called Methyl Alcohol or “Wood Alcohol”), with consequential risk 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/TMd730r6Sxc

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/asiaticon-sa-de-cv-issues-voluntary-nationwide-recall-v-klean-hand-sanitizer-gel-medically-minded

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

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SkinGuard24 All Day Hand Sanitizer Recall [US]

SkinGuard24 All Day Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: SG24 LLC, Bolingbroke, Georgia establishment, recalls certain batch/lots of SkinGuard24 – All Day Hand Sanitizer products from the American marketplace due to the suspected presence of Methanol (also called Methyl Alcohol or “Wood Alcohol”), with consequential 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/VtfT30r5dTS

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sg24-llc-issues-voluntary-nationwide-recall-skinguard24-hand-sanitizer-labeled-contain-methanol

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

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Jaloma Antiseptic Hand Sanitizer Recall [US]

US FlagUS/Silver Spring: Jaloma branded Antiseptic Hand SanitizerLaboratorios Jaloma SA de CV, a Guadalajara, Jalisco, Mexico establishment, recalls certain batch/lots of Jaloma Antiseptic Hand Sanitizer products from the American marketplace due to the suspected presence of Methanol (also called Methyl Alcohol or “Wood Alcohol”), with consequential risk 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/E4Jh30r3uyX

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/laboratorios-jaloma-sa-de-cv-issues-voluntary-recall-jaloma-antiseptic-hand-sanitizer-due-potential

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

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Triangle Tube Prestige Gas Boiler Recall [US & Canada]

Triangle Tube Prestige Condensing Gas Boilers Recall [US & Canada]

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US FlagCanada FlagUS/Washington & Canada/Ottawa: Triangle Tube/III Co., Inc., a West Deptford, New Jersey establishment recalls an estimated total of 69,600 Prestige Solo & Prestige Excellence Condensing Gas Boilers (approximately 63,000 in the US and approximately 6,600 in Canada) from the American and Canadian marketplaces due to possible Vent Adapter detachment and consequential risks of Carbon Monoxide poisoning, respiratory depression, nausea, confusion, cardiac arrhythmia, seizures and death, all serious health and safety hazards.

CPSC: http://ht.ly/Tm0l30r2VjI; HCSC: http://ht.ly/VyjO30r2VjL

Direct US link: https://www.cpsc.gov/Recalls/2020/Triangle-Tube-Recalls-to-Repair-Gas-Boilers-Due-to-Risk-of-Carbon-Monoxide-Hazard-One-Death-Reported-In-Home-Remedy-May-Be-Delayed-Due-To-COVID-19-Restrictions

Direct Canada link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73415r-eng.php

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves twenty-two (22) models of the Prestige Solo & Prestige Excellence Condensing Gas Boiler manufactured between November 2011 and October 2019 sold, marketed and installed for residential and light commercial use.

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Herbacil Antiseptic Hand Sanitizer Recall [US]

Herbacil Antiseptic Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: Broncolin S.A. de C.V., an Iztacalco, Mexico establishment, recalls certain batch/lots of Herbacil Antiseptic branded Hand Sanitizer products from the American marketplace due to the suspected presence of Methanol (also called Methyl Alcohol or “Wood Alcohol”), with consequential risk 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/cZar30r2DEH

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/broncolin-sa-de-cv-issues-voluntary-nationwide-recall-herbacil-antiseptic-hand-sanitizer-70-alcohol

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

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