Primus Pharma Limbrel Medical Food Recall [US]

US FlagUS/Silver Spring: Primus Pharma Limbrel Medical Food Recall [US]Primus Pharmaceuticals, Inc., a Scottsdale, Arizona establishment, recalls all unexpired batch/lots of Limbrel Medical Food products due to suspected
rare but serious and side effects, all serious health hazard. FDA: http://ht.ly/zotI30i64Fy

Direct link: https://www.fda.gov/Safety/Recalls/ucm594357.htm

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

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Magno-Humphries Basic Drugs Senna Laxative Recall [US]

US FlagUS/Silver Spring: 9689 - FDA - Magno-Humphries Labs Basic Drugs Senna Laxative Recall [US]Magno-Humphries Laboratories, Inc. recalls certain batch/lots of Basic Drugs branded Senna Laxative due to mislabeling, suspected presence of Naproxen Sodium, a non-steroidal anti-inflammatory drug (“NSAID”) and consequential risk of fatal adverse events in patients with underlying illnesses, all serious health and safety hazards. FDA: http://ht.ly/7dqq30hW0VE

Direct link: https://www.fda.gov/Safety/Recalls/ucm593150.htm

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

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Marmex Blue Pearl Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: Marmex Blue Pearl Nutritional Supplement Recall [US]Marmex Corporation, an Orange, California establishment, recalls all current batch/lots of Blue Pearl All Natural Male Enhancement Supplements due to undeclared Sildenafil, an active ingredient in an FDA-approved prescription drug used to treat male sexual dysfunction, making this product a new drug for which safety and efficacy has not been established, all serious health and safety hazards. FDA: http://ht.ly/sr0230hew4f

Direct link: https://www.fda.gov/Safety/Recalls/ucm588969.htm

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

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Synodrin Pain Relieving Cream Recall [US]

US FlagUS/Washington: Synodrin Pain Relieving Cream Recall [US]Natural Solutions for Life recalls an estimated 56,000 units of Synodrin Pain Relieving Cream due to suspected failure to comply with federal Child Resistant Closure Requirements in contravention of the US Poison Prevention Packaging Act, all serious health and safety hazards. CPSC: http://ht.ly/cNvT30h7CpZ

Direct link: https://www.cpsc.gov/Recalls/2018/Natural-Solutions-for-Life-Recalls-Synodrin-Pain-Relieving-Cream-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirement#

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports the recalled Synodrin Lidocaine Maximum Strength Pain Relieving Cream sold in a white jar with a blue label with the phrase, “Synodrin Lidocaine Maximum Strength 4% Pain Relieving Cream” printed on the front.

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Pharmacist Choice Alcohol Prep Pad Recall [US]

US FlagUS/Silver Spring: Pharmacist Choice Alcohol Prep Pad Recall [US]Simple Diagnostics, Inc. recalls certain batch/lots of Pharmacist Choice Alcohol Prep Pads due to suspected failure to assure sterility, other quality issues and consequential risk of bacterial infection, a serious health hazard. FDA: http://ht.ly/7XUy30h5fjp

Direct link: https://www.fda.gov/Safety/Recalls/ucm587680.htm

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

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Alesse 21 & Alesse 28 Birth Control Pill Recall [Canada]

Canada FlagCanada/Ottawa: Alesse 21 & Alesse 28 Birth Control Pill Recall [Canada]Health Canada warns consumers, physicians and other healthcare professionals that certain batch/lots of Alesse 21 and Alesse 28 Oral Contraceptive Tablets may suffer from component breakage, risk of smaller dosage and possible failure to prevent pregnancy, all serious health and safety hazards. HCSC: http://ht.ly/yJah30h4Cyi

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/65306a-eng.php

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

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Bull & Chao Jimengnan Dietary Supplement Recall [US]

US FlagUS/Silver Spring: Bull & Chao Jimengnan Dietary Supplement Recall [US]Nutra Labs Inc. recalls certain batch/lots of Bull and Chao Jimengnan Dietary Supplements due to suspected presence of Sildenafil, an FDA approved product used to treat Erectile Dysfunction, making Bull capsules and Chao Jimengnan tablets unapproved new drugs, a serious health hazard. FDA: http://ht.ly/yxUG30gW3CV

Direct link: https://www.fda.gov/Safety/Recalls/ucm587141.htm

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

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