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Pharmacy, psychiatry and family practice personnel are informed by the FDA that one lot of 30-count Effexor XR (venlafaxine HCl) 150 mg extended-release...
The FDA informs pulmonology, infectious disease, and pharmacy personnel that Dirobax (Doripenem) carries an increased risk of death and notes that it...
Pharmacy professionals are informed by the FDA that one lot of Baxter International DIANEAL PD-2 Peritoneal Dialysis Solution with 1.5% Dextrose 6000...
Cardiology, surgery personnel and risk managers are informed by the FDA that a safety advisory has been issued concerning HeartMate II LVAS Pocket System...
Consumers have been informed by the FDA that dietary supplements for sexual enhancement by Atlas Operations, Inc. have been recalled because they were...
The FDA informs risk managers and biomedical engineering personnel that GE Healthcare resuscitation systems (Panda, Giraffe, and others) are recalled...
Risk Managers are informed by the FDA that ACME Monaco Guidewire .035×150 3 MMJ TCFC, item number 88241, is recalled (Class I) because various convenience...
The FDA informs risk managers and biomedical engineering personnel that ISIS HVT tracheal tube cuffed with subglottic secretion suction port by Teleflex...
An accidental overdose of Tylenol (acetaminophen) can cause liver failure in unsuspecting users with an array of adverse outcomes. Over-the-Counter Tylenol...
Testosterone replacement therapy winds up causing cardiovascular disease in many men who take the popular drug. Testosterone Gel Lawsuits Are on the Rise...
Biomedical engineering, nursing, critical care medicine, risk managers, and home care personnel are informed by the FDA that approximately 600 Trilogy...
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[...] Sulfate Inhalation Solution, 0.083% due to results from an internal monitoring process. FDA Alert on Albuterol Sulfate Inhalation Solution, 0.083% The specific product passed the aseptic process [...]
[...] cartridges, by Tandem Diabetes Care, are recalled due to the risk of leaking. FDA Alert on T:slim Insulin Cartridges FDA’s reason for the recall is that the affected [...]
[...] Rohto Cool eye drops, by The Mentholatum Company, are recalled due to sterility control review. FDA Alert on Rohto Eye Drops FDA’s reason for the recall is based on a manufacturing review at the [...]
[...] Corporation, are recalled because the product was found to contain undeclared milk. FDA Alert on StemAlive 90 Capsules FDA’s reason for the recall is that StemAlive 90 capsules were [...]
[...] are informed by the FDA that one lot of P-Boost and NatuRECT is recalled due to undeclared drug ingredient. Background of P-Boost and NatuRECT P-Boost and NatuRECT, by Tendex, are marketed as [...]
[...] . FDA Alert on Adipotrim XT FDA’s […] The post Adipotrim XT Recalled due to Undeclared Drug Ingredient appeared first on - AttorneyOne.com - Finding An Attorney Online, Just Got Easier. [...]
[...] informed by the FDA that one lot of Burn 7 capsules by Deseo Rebajar is recalled due to undeclared drug ingredient. FDA Alert on Burn 7 Capsules FDA’s reason for the recall is that Lot No. [...]
[...] […] The post Dream Body Slimming Capsule: FDA Notification Not to Use due to Undeclared Drug Ingredient appeared first on - AttorneyOne.com - Finding An Attorney Online, Just Got Easier. [...]
[...] . FDA Alert on VitaliKOR […] The post VitaliKOR Fast Acting Recalled due to Undeclared Drug Ingredients appeared first on - AttorneyOne.com - Finding An Attorney Online, Just Got Easier. [...]
[...] marketed […] The post Rhino 5 Plus, Maxtremezen and Extenzone Recalled due to Undeclared Drug Ingredients appeared first on - AttorneyOne.com - Finding An Attorney Online, Just Got Easier. [...]
[...] healthcare professionals and consumers that two lots of RezzRX are recalled due to undeclared drug ingredients. Background of RezzRX RezzRX, by Fossil Fuel Products LLC, is promoted as a natural [...]
[...] ” Extenze, and New XZen Platinum Marketed as Dietary Supplements Recalled due to Undeclared Drug Ingredients appeared first on - AttorneyOne.com - Finding An Attorney Online, Just Got Easier. [...]
[...] The FDA warns cardiology, radiology and pharmacy personnel that the use of Lexiscan (regadenoson) and Adenoscan (adenosine) has been related to rare [...]
[...] Emergency medicine and pharmacy personnel are informed by the FDA that the agency is aware of certain Meridian Medical Technologies [...]
[...] Family physicians, pharmacy personnel and consumers are informed by the FDA that 20 lots of Abbott’s FreeStyle and [...]
[...] The FDA informs hematology and pharmacy personnel that two lots of Soliris (Eculizumab) concentrated solution for intravenous infusion, by [...]
[...] of Pro ArthMax Pro ArthMax, by Human Science Foundation, is promoted as a dietary supplement for joint, muscle and arthritic pain. In Korean the name of the product is & [...]
[...] Capsules MasXtreme Capsules, by Natural Wellness Inc., were sold in blister packs as dietary supplement. FDA Alert on MasXtreme Capsules FDA’s reason for the recall is that MasXtreme [...]
[...] drug ingredient. Background of Prolatis’ Prolatis’ was marketed as dietary supplement. FDA Alert on Prolatis’ FDA’s reason for the recall was that Prolactis’ [...]
[...] adverse events. Background of TimeOut Capsules TimeOut capsules are marketed as dietary supplement for sexual enhancement. FDA Alert on TimeOut Capsules The US FDA analyzed TimeOut capsules [...]
[...] The FDA informs risk managers and cardiology personnel that the Embol-X Glide Protection System is recalled due to a deformed cannula tip that [...]
[...] The FDA informs risk managers and cardiology personnel that the TorFlex Transseptal Guiding Sheath Kit is recalled because the sheath could [...]
[...] The FDA informs risk managers, critical care medicine and cardiology personnel that one lot of Baxter’s Nitroglycerin in 5% Dextrose is recalled due to particulate [...]
[...] Health professionals, cardiology personnel, and risk management personnel are informed by the FDA that Medtronic Interventional [...]
[...] Pediatrics, pharmacy healthcare personnel, consumers and patients are informed by the FDA that 18 batches of Perrigo [...]
[...] Dermatology, neurology, and pharmacy healthcare personnel are informed by the FDA that Onfi (clobazam) can cause rare but serious skin reactions [...]
[...] Medical geneticist, pediatrics, and pharmacy healthcare personnel are informed by the FDA that there have been adverse event reports associated with [...]
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[...] Recalled due to Microbial Contamination appeared first on - AttorneyOne.com - Finding An Attorney Online, Just Got Easier. [...]
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