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Category Archives: Consumer Products
Vitaflo USA Renastart Recall
Vitaflo USA Renastart: Recall – Possible Health Risk Due To Incorrectly Labeled Cans AUDIENCE: Pediatrics, Health Professionals, Consumers ISSUE: Vitaflo USA has announced a voluntary recall of Renastart 14.11 oz (400g) cans, Batch Number 12832, because some of the product … Continue reading
Posted in Consumer Products, FDA Recall, Pediatrics
Tagged Consumers, drug risks, FDA recall, Pediatrics, Recall, Renastart, Vitaflo USA, Vitaflo USA Renastart Recall
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Perfect Image Solutions Topical Hair Regrowth Products Recall
Perfect Image Solutions Topical Hair Regrowth Products: Recall – Unapproved Drugs, Risk of Health Hazards Men’s Minoxidil 15% Azelaic 5% Hair regrowth topical, 60ml Men’s Minoxidil 10% Azelaic 5% Hair regrowth topical, 60mL Men’s Minoxidil 5% Azelaic 5% Hair regrowth … Continue reading
Posted in Consumer Products, FDA 2012, FDA Recall
Tagged Consumer Products, drug risks, FDA recall, Hair regrowth topical, Men's Minoxidil, Perfect Image Solutions, Perfect Image Solutions Topical Hair Regrowth Products Recall, Recall, Topical Hair Regrowth Products, unapproved new drugs, Women's Minoxidil
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Vagifresh Ball Vagifresh Gel Female One Recall
Vagifresh Ball, Vagifresh Gel, Female One: Recall – Undeclared Drug Ingredient, Bacterial Contamination AUDIENCE: Consumer, OB/GYN ISSUE: USA Far Ocean Group Inc. notified the public of a recall of Vagifresh Ball and Vagifresh Gel, sold as cosmetics. Vagifresh Gel was found … Continue reading
Posted in Consumer Products, FDA 2012, FDA Recall, FDA Warning, OBGYN
Tagged Bacterial Contamination, drug, drug risks, fda, FDA notice, FDA recall, FDA warning, Female One, OBGYN, Recall, Undeclared Drug Ingredient, USA Far Ocean Group Inc, Vagifresh Ball, Vagifresh Ball Vagifresh Gel Female One Recall, Vagifresh Gel
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Endo Pharmaceuticals Opiate Products by Novartis Consumer Health
Endo Pharmaceuticals Opiate Products by Novartis Consumer Health: Public Health Advisory – Potential Safety Risk Including the following products: Opana ER (oxymorphone hydrochloride) Extended-Release Tablets CII Opana (oxymorphone hydrochloride) CII Oxymorphone hydrochloride Tablets CII PERCOCET (oxycodone hydrochloride and acetaminophen USP) … Continue reading
Posted in Consumer Products, FDA 2011, FDA Warning, Pharmacy
Tagged drug risks, Endo Pharmaceuticals .Opiate Products. Novartis Consumer Health, Endo Pharmaceuticals Opiate Products by Novartis Consumer Health, ENDOCET, ENDODAN, FDA notice, FDA warning, MORPHINE SULFATE, Opana, Opana ER, Oxymorphone, PERCOCET, PERCODAN, ZYDONE
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Novartis Exedrin Bufferin Gas-X Prevention NoDoz Recall
Novartis Consumer Health Over-The-Counter Products: Recall – Potential Presence of Foreign Tablets or Chipped or Broken Tablets or Gelcaps including Excedrin, NoDoz, Bufferin, Gas-X Prevention AUDIENCE: Consumer, Pharmacy ISSUE: Novartis Consumer Health Inc. is voluntarily recalling all lots of over-the-counter … Continue reading
Posted in Consumer Products, FDA 2011, FDA Recall, Pharmacy
Tagged Bufferin, drug risks, Exedrin, FDA recall, Gas-X Prevention, NoDoz, Novartis, Novartis Exedrin Bufferin Gas-X Prevention NoDoz Recall, Recall
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Over-the-Counter (OTC) Liquid acetaminophen FDA Notice
Liquid Acetaminophen Concentration FDA Notice AUDIENCE: Pediatrics, Consumers, Pharmacy ISSUE: The FDA is informing the public that an additional concentration of liquid acetaminophen marketed for “infants” (160 mg/5 mL) is now available. This change in the concentration will affect the … Continue reading
Posted in Consumer Products, FDA 2011, FDA Notice, Pediatrics, Pharmacy
Tagged Children Medicines, Drug Safety Communication, FDA notice, Infant/Pain Reliever, Liquid acetaminophen, Little Fevers, Over-the-Counter (OTC), Over-the-Counter (OTC) Liquid acetaminophen, Pedia Care, safety label changes, Triaminic, Triaminic Infants’ Syrup Fever Reducer Pain Reliever, Tylenol
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Eclectic Institute Dietary Supplements Goto Kola Bladderwrack Recall
Eclectic Institute Dietary Supplements: Recall – Possible Salmonella Contamination Include the products Gotu Kola (Centella Asiatica), Bladderwrack (Fucus Vesiculosus) AUDIENCE: Consumer ISSUE: Eclectic Institute is voluntarily recalling specific lots of its freeze-dried capsules containing Gotu Kola (Centella asiatica) and Bladderwrack … Continue reading
Posted in Consumer Products, FDA 2011, FDA Recall
Tagged Bladderwrack, Consumer Products, Drug Safety Communication, Eclectic Institute Dietary Supplements, FDA recall, Goto Kola, Recall
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