The move comes after a study by the US Food and Drug Administration revealed that NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. January 15, 2021 -- The U.S. Food and Drug Administration is alerting health care professionals to labeling updates for the preparation of vinca alkaloids, a... January 08, 2021 -- Fresenius Kabi USA is voluntarily recalling a single lot of Ketorolac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial... January 4, 2021 -- Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol in 33.81 oz. Withdrawn from US in 2005. Side effects are observed NOT tested. This can lead to... October 05, 2020 -- Marksans Pharma Limited, India is voluntarily expanding its earlier initiated recall on June 05, 2020 to include an additional 76 unexpired... ISSUE: FDA is warning that taking higher than recommended doses of the common over-the-counter (OTC) allergy medicine Benadryl (diphenhydramine) can lead to... ISSUE: The FDA is requiring the Boxed Warning, FDA’s most prominent warning, be updated by adding other information to the prescribing information for... Whatever your topic of interest, subscribe to our newsletters to get the best of Drugs.com in your inbox. Select one or more newsletters to continue. Voluntarily withdrawn from market by Lily. Expands Voluntary Nationwide Recall of Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Due to Microbial Contamination, Shane Erickson, Inc. DBA Innovative Marketing Consultants Issues Voluntary Nationwide Recall of Wash-Free Hand Sanitizer Due to Potential Presence of Undeclared Methanol, AvKARE Issues Voluntary Nationwide Recall of Sildenafil 100mg Tablets and Trazodone 100mg Tablets Due to Product Mix-Up, Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Anagrelide Capsules, USP Due to Dissolution Test Failure, FDA Alerts Healthcare Professionals About the Risk of Medication Errors with Tranexamic Acid Injection Resulting in Inadvertent Intrathecal (Spinal) Injection, MPM Medical LLC Issues Voluntary Nationwide Recall of Regenecare HA Hydrogel Due to Burkholderia cepecia Contamination, Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine, Lohxa LLC Issues Voluntary Nationwide Recall of Chlorhexidine Gluconate Oral Rinse USP, 0.12% Due to Microbial Contamination, Nostrum Laboratories, Inc. Issues Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 500 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit, Nostrum Laboratories, Inc. Issues Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 750 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit, Sunstar Americas Inc. Issues Voluntary Nationwide Recall of Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Due to Microbial Contamination, Drug Safety Communication: Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) - Avoid Use of NSAIDs in Pregnancy at 20 Weeks or Later, Marksans Pharma Limited Issues Expansion of Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets, USP 500mg & 750mg, Due to the Detection of N-Nitrosodimethylamine (NDMA), Drug Safety Communication: Benadryl (diphenhydramine) - Serious Problems with High Doses of the Allergy Medicine, Drug Safety Communication: Benzodiazepine Drug Class - Boxed Warning Updated to Improve Safe Use. A list of drugs withdrawn from the US market for safety reasons was generated, along with the corresponding period of time each drug was marketed. tablet; withdrawn because of risk of cancer and kidney disease, Withdrawn in many countries because of risk of fatal, rhesus rotavirus vaccine-tetravalent (RotaShield), Risk of heart attacks and death. Some drugs in this list (e.g. This drug continues to be available in the US. Several drugs are either banned or withdrawn after introduction in the market. Expands Voluntary Nationwide Recall of Paroex® Chlorhexidine Gluconate Oral Rinse … This NSAID was on the market for less than a year (342 days). Cardiac valvular disease, pulmonary hypertension, cardiac fibrosis; Increased mortality at higher doses; increased hospitalizations. Drugs WRITEN by LAIMA JONUSIENE to prove that the drug companies make mistakes with our lives we this! Illegal drugs, in reverse order: 10 million worth of it worldwide the year the! 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