EU issues 45 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 42/2020 of its Rapid Alert System containing forty-five (45) 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/gQWO30rfffx

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000016&Year=2020&lng=en

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Lidl Cologran Sucralose Sweetener Recall [UK]

Lidl Cologran Sucralose Sweetener Recall [UK]

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UK FlagUK/London: Lidl Great Britain Limited (“Lidl GB”), a London, England establishment and subsidiary of Lidl of Stiftung & Co KG of Neckarsulm, Baden-Wüttenberg, Germany, recalls a certain batch/lot of Cologran Sucralose Sweetener Tablets from the British marketplace due to undeclared Aspartame (also known as E951). This artificial sweetener is made with the chemical Phenylalanine poses as serious health and safety hazards for people with Phenylketonuria (also called “PKU”) as well as people taking certain medications for their mental health.

FSA: http://ht.ly/QuSj30rfbNB

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-47-2020

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

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EU issues 32 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 41/2020 of its Rapid Alert System containing thirty-two (32) 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/bU7b30re3Nm

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000015&Year=2020&lng=en

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Lidl Cologran Stevia Sweetener Recall Update [UK]

Lidl Cologran Stevia Sweetener Tablet Recall [UK]

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UK FlagUK/London: Lidl Great Britain Limited (“Lidl GB”), a London, England establishment and subsidiary of Lidl of Stiftung & Co KG of Neckarsulm, Baden-Wüttenberg, Germany, updates its existing recall for a single batch/lot of Cologran Stevia Sweetener Tablets, a Stevia variant, from the British marketplace to include additional batch/lots.

The original recall was initiated due to undeclared Aspartame (also known as E951), an artificial sweetener made with the chemical Phenylalanine and consequential possible Carcinogenic risks as well as serious health and safety hazards for people with Phenylketonuria (also called “PKU”) as well as people taking certain medications for their mental health.

FSA: http://ht.ly/Q5sc30reuRc

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-45-2020-update-1

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

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EU issues 26 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 40/2020 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/ue6U30rdjeo

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=10000014&Year=2020&lng=en

Additional information:
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Lidl Cologran Stevia Sweetener Recall [UK]

Lidl Cologran Stevia Sweetener Tablet Recall [UK]

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UK FlagUK/London: Lidl Great Britain Limited (“Lidl GB”), a London, England establishment and subsidiary of Lidl of Stiftung & Co KG of Neckarsulm, Baden-Wüttenberg, Germany, recalls certain batch/lots of Cologran Stevia Sweetener Tablets, a Stevia variant, from the British marketplace due to undeclared Aspartame (also known as E951), an artificial sweetener made with the chemical Phenylalanine and consequential possible Carcinogenic risks as well as serious health and safety hazards for people with Phenylketonuria (also called “PKU”) as well as people taking certain medications for their mental health.

FSA: http://ht.ly/GvaK30rcpbw

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-45-2020

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

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EU issues 30 Product, Toy & Vehicle Recalls

European Union FlagBelgium/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:
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Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Lupin Pharmaceuticals, Inc., a Baltimore, Maryland establishment, recalls all current batch/lots of Lupin Pharma branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/NuJP30qY97Z

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntarily-nationwide-recall-metformin-hydrochloride-extended

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

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Granules Pharma Metformin Hydrochloride Recall [US]

Granules Pharma Metformin Hydrochloride Recall [US]

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US FlagUS/Silver Spring: Granules Pharmaceuticals, Inc., a Chantilly, Virginia establishment, recalls twelve (12) batch/lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/dXLm30qX5hG

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/granules-pharmaceuticals-inc-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended

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

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EU issues 28 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 25/2020 of its Rapid Alert System containing twenty eight (28) 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/nClr30qSbyo

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=26&Year=2020&lng=en

Additional information:
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Apotex Metformin Hydrochloride Tablet Recall [Canada]

Apotex Metformin Hydrochloride Tablet Recall [US]

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Canada FlagCanada/Ottawa: Apotex Corp., a Toronto, Ontario establishment, recalls certain batch/lots of Apotex Corp branded Metformin Hydrochloride Extended-Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable Health Canada levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

HCSC: http://ht.ly/RIm630qRn75

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/73339r-eng.php

Additional information:
The Health Canada (“HCSC) reports the following Metformin medications are subject to this recall:

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Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Lupin Pharmaceuticals, Inc., a Baltimore, Maryland establishment, recalls certain batch/lots of Lupin Pharma branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/GfnZ30qQfdN

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntarily-nationwide-recall-one-lot-metformin-hydrochloride

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

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EU issues 33 Product, Toy & Vehicle Recalls

European Union FlagBelgium/Brussels: The European Union issues Report 24/2020 of its Rapid Alert System containing thirty three (33) 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/Ul6b30qPoLQ

Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=25&Year=2020&lng=en

Additional information:
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Apotex Metformin Hydrochloride Tablet Recall [US]

Apotex Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Apotex Corp., a Toronto, Ontario establishment, recalls certain batch/lots of Apotex Corp branded Metformin Hydrochloride Extended-Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/HmUE30qPhSK

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended-release-tablets

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

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Actavis Pharma Metformin Hydrochloride Tablet Recall [US]

Actavis Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Teva Pharmaceuticals USA, Inc., a Parsippany, New Jersey establishment and subsidiary of Teva Pharmaceutical Industries Ltd. of Petah Tikva, Israel, recalls certain batch/lots of Actavis Pharma, Inc. branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/q9Pu30qOed1

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-inc-initiates-voluntary-nationwide-recall-metformin-hydrochloride-extended

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

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