M1 Alpha & Sten Z Supplement Recall [US]

US FlagUS/Silver Spring: Andropharm M1 Alpha & Sten Z Supplement Recall [US]Andropharm recalls certain batch/lots of M1 Alpha and Sten Z Supplements due to suspected presence of Anabolic Steroids and consequential risk of a wide range of life-affecting injuries and/or conditions, all serious health hazards. FDA: http://ht.ly/mj1b30dyBbI

Direct link: https://www.fda.gov/Safety/Recalls/ucm566553.htm

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

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Ultra-Sten and D-Zine Supplement Recall [US]

US FlagUS/Silver Spring: Ultra-Sten and D-Zine Supplement Recall [US]Hardcore Formulations recalls all current batch/lots of Ultra-Sten and D-Zine Dietary Supplements due to suspected presence of Anabolic Steroids and consequential risk of a wide range of life-affecting injuries and/or conditions, all serious health hazards. FDA: http://ht.ly/g4Ee30dtRDE

Direct link: https://www.fda.gov/Safety/Recalls/ucm565827.htm

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

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Bayer RestoraLAX Recall Expands [Canada]

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Canada/Ottawa: Bayer RestoraLAX Recall Expands [Canada]Bayer Inc. expands its existing recall for certain batch/lots of RestoraLAX to include additional Laxative varieties due to the presence of clumps or lumps in the product and consequential choking hazard. HCSC: http://ht.ly/BT6F30dtmFS

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/63908a-eng.php

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

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Bayer RestoraLAX Laxative Recall [Canada]

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Canada/Ottawa: Bayer RestoraLAX Recall [Canada]Bayer Inc. recalls certain batch/lots of RestoraLAX Laxative due to presence of unexpected clumps or lumps in the product and consequential choking hazard. HCSC: http://ht.ly/fftt30dlGl3

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/63798a-eng.php

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

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Bristol-Myers Squibb Eliquis Recall Update [US]

US FlagUS/Silver Spring: Bristol-Myers Squibb Eliquis Recall [US]Bristol-Myers Squibb updates its existing recall for one (1) batch/lots of Eliquis (apixaban) 5 mg Tablets due to suspected incorrect dosage packaging and consequential failure to protect against serious and life-changing cardiovascular events and/or Death, all serious health hazards. FDA: http://ht.ly/CpHA30cGw9G

Direct link: https://www.fda.gov/Safety/Recalls/ucm563547.htm

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

Bristol-Myers Squibb Eliquis Recall [US]

US FlagUS/Silver Spring: Bristol-Myers Squibb Eliquis Recall [US]Bristol-Myers Squibb recalls one batch/lots of Eliquis (apixaban) 5 mg Tablets due to suspected incorrect dosage packaging and consequential failure to protect against serious and life-changing cardiovascular events and/or Death, all serious health hazards. FDA: http://ht.ly/7WzT30cB77V

Direct link: https://www.fda.gov/Safety/Recalls/ucm563002.htm

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

Valpam 5 (Diazepam) Tablet Recall [Australia]

Australia FlagAustralia/Canberra: Logo - Arrow PharmaArrow Pharma Pty Ltd. recalls all current batch/lots of Valpam 5 (diazepam) 5mg Tablets due to suspected presence of an incorrect drug and consequential insufficient or overdose drug dosage conditions, all serious health hazards. ACCC: http://ht.ly/u0AT30czEwa

Direct link: https://www.productsafety.gov.au/recall/arrow-pharma-pty-ltd-valpam-5-diazepam-5mg-tablets-in-50-tablet-blister-packs

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

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