FDA: Several Companies Recall Metformin ER Over NDMA Concerns By Brian Park, PharmD Publish Date July 14, 2020
FDA: Risk of Methanol Toxicity With Certain Hand Sanitizers By Diana Ernst, RPh Publish Date July 6, 2020
Supplements With Undeclared Active Ingredients Pose Substantial Health Risk By Cassandra Pardini, PharmD Publish Date June 25, 2020
OTC Cough/Cold Meds Recalled Due to Incorrect Dosing Cups By Brian Park, PharmD Publish Date June 23, 2020
FDA Revokes EUA for COVID-19 Antibody Test, Cracks Down on Fraudulent At-Home Tests By Diana Ernst, RPh Publish Date June 18, 2020
Warning Letters Issued to Several Companies Selling Unapproved “Homeopathic” Injectables By Diana Ernst, RPh Publish Date June 18, 2020
FDA: Vial Caps of Two Neuromuscular Blocking Agents May Not Have Warning Statement By Brian Park, PharmD Publish Date June 4, 2020
FDA: Certain Epinephrine Autoinjector Devices May Have Missing Safety Component By Brian Park, PharmD Publish Date June 2, 2020
FDA: Unacceptable NDMA Levels Identified in Certain Metformin ER Products By Diana Ernst, RPh Publish Date May 29, 2020
Superpotent Lots of Hypothyroidism Treatment NP Thyroid Recalled By Brian Park, PharmD Publish Date May 27, 2020
Unapproved Cannabidiol, Curcumin Injectables Marketed for Multiple Disorders Recalled By Brian Park, PharmD Publish Date May 22, 2020
Recall: Undeclared Antihypertensive Found in Compounded Hair Loss Drug By Brian Park, PharmD Publish Date May 14, 2020
Fiber Supplements Recalled Due to Possible Plastic Contamination By Brian Park, PharmD Publish Date April 30, 2020
FDA Issues Safety Alert Regarding Use of Hydroxychloroquine, Chloroquine for COVID-19 By Diana Ernst, RPh Publish Date April 24, 2020
Pain Medication Recalled Due to Presence of Particulate Matter in Vials By Brian Park, PharmD Publish Date April 22, 2020
Amneal’s Nizatidine Oral Solution Recalled Due to NDMA Concerns By Brian Park, PharmD Publish Date April 20, 2020
FDA: All Ranitidine Products Must Be Removed From the Market By Brian Park, PharmD Publish Date April 1, 2020
Phytonadione Injectable Emulsion Ampules Recalled Following Reports of Glass Injuries By Brian Park, PharmD Publish Date March 27, 2020
Certain Blister Packages of Sandimmune, Neoral Not Child Resistant By Diana Ernst, RPh Publish Date March 19, 2020
FDA, FTC Crack Down on Fraudulent COVID-19 “Treatments” By Diana Ernst, RPh Publish Date March 10, 2020
FDA Strengthens Warning About Risk of Neuropsychiatric Events With Montelukast By Diana Ernst, RPh Publish Date March 5, 2020
Phenytoin Oral Suspension Recalled Due to Potential for Inaccurate Dosing By Brian Park, PharmD Publish Date February 24, 2020
FDA: Bacitracin for Injection to Be Withdrawn From Market By Brian Park, PharmD Publish Date February 3, 2020
FDA: Serious Complications Following Clozapine-Induced Constipation By Diana Ernst, RPh Publish Date January 29, 2020
FDA: Possible Cybersecurity Issues With Certain Patient Monitoring Devices By Steve Duffy Publish Date January 27, 2020
Lamotrigine Recalled Due to Cross-Contamination With Hypertension Med By Brian Park, PharmD Publish Date January 13, 2020
Recall: NDMA Identified in Mylan’s Nizatidine Capsules By Diana Ernst, RPh Publish Date January 8, 2020
FDA: Cases of Respiratory Depression With Gabapentinoids Reported By Diana Ernst, RPh Publish Date December 19, 2019
FDA: Do Not Use Products Distributed by Basic Reset, Biogenyx By Steve Duffy Publish Date December 11, 2019
FDA: Dollar Tree Stores May Be Selling Potentially Harmful OTC Products By Brian Park, PharmD Publish Date November 15, 2019
FDA: Biotin Interference Still Concerning, Particularly With Troponin Tests By Diana Ernst, RPh Publish Date November 6, 2019
FDA: Testing Reveals Unacceptable Levels of NDMA in Two H2 Blockers By Brian Park, PharmD Publish Date November 4, 2019
Potential Presence of Foreign Substance Prompts Recall of Anti-Anxiety Med By Brian Park, PharmD Publish Date October 28, 2019
Recall: Small Amounts of Asbestos Identified in Baby Powder By Brian Park, PharmD Publish Date October 18, 2019
CVS Suspends Sale of Zantac, OTC Generic as More Ranitidine Recalls Announced By Brian Park, PharmD Publish Date October 1, 2019
Maker Halts Distribution of Generic Zantac Due to Possible Carcinogen Publish Date September 20, 2019
FDA: Nitrosamine Impurity Identified in Commonly Used Acid Suppressant By Diana Ernst, RPh Publish Date September 13, 2019
Recall of All Doses of Parathyroid Hormone Natpara Issued By Brian Park, PharmD Publish Date September 6, 2019
Cancer Risk From Recalled ARBs “Likely Much Lower” Than Initially Estimated, Says FDA By Brian Park, PharmD Publish Date September 3, 2019
CDC Issues Warning About Cases of Severe Pulmonary Disease Linked to E-Cigarette Use By Diana Ernst, RPh Publish Date September 3, 2019
Losartan, Ezetimibe Recall Initiated Due to Bottles Not Being Child Resistant By Brian Park, PharmD Publish Date August 30, 2019
Class I Recall Issued for Transcatheter Heart Valve Delivery System By Steve Duffy Publish Date August 22, 2019
FDA: Entacapone Not Associated With Increased Prostate Cancer Risk By Brian Park, PharmD Publish Date August 13, 2019
FDA Warns of “Cure-All” Products That Actually Contain Bleach By Brian Park, PharmD Publish Date August 13, 2019
FDA Recalls Herbal Meds Being Marketed for Various Diseases By Steve Duffy Publish Date July 29, 2019
Boxed Warning Added to Tofacitinib Prescribing Information By Diana Ernst, RPh Publish Date July 26, 2019
Certain Breast Implants, Tissue Expanders Recalled Due to Cancer Link By Steve Duffy Publish Date July 24, 2019
Oral Contraceptive Recalled Due to Possibility of Reduced Efficacy By Steve Duffy Publish Date July 24, 2019
Recall: Vials Labeled as Kogenate FS Contain Another Hemophilia A Treatment By Brian Park, PharmD Publish Date July 22, 2019
Recall Of Multiple Rx, OTC Ophthalmic Products Announced By Brian Park, PharmD Publish Date July 16, 2019
Several Ophthalmic Products Recalled Due to Possible Sterility Issues By Brian Park, PharmD Publish Date July 3, 2019
Hydromorphone Injection Recalled Due to Presence of Sulfite By Diana Ernst, RPh Publish Date July 3, 2019
Phase 3 Study Evaluating Novel Therapy for Pancreatic Cancer Discontinued By Brian Park, PharmD Publish Date July 2, 2019
Fluorouracil Injection Recalled Due to Glass Particulate By Brian Park, PharmD Publish Date July 2, 2019
FDA: Potential Cybersecurity Risks With Certain Insulin Pumps By Brian Park, PharmD Publish Date June 28, 2019
FDA: Dietary Supplement Ingredient May Potentially Cause Miscarriage, Fetal Harm By Steve Duffy Publish Date June 4, 2019
FDA Issues Diabetes Device Warning After Serious Adverse Event By Steve Duffy Publish Date May 17, 2019
Promacta Oral Suspension Recalled Due to Possible Peanut Contamination By Diana Ernst, RPh Publish Date May 13, 2019
Injectable Pain Med Recalled Due to Possible Microbial Contamination By Steve Duffy Publish Date May 1, 2019
FDA: Boxed Warning, Contraindication Added to Several Insomnia Medications By Steve Duffy Publish Date April 30, 2019
Fentanyl Transdermal Patches Recalled Due to Product Mislabeling By Steve Duffy Publish Date April 22, 2019
FDA Warns Against the Use of Unapproved Devices Marketed for Assessing Head Injury By Steve Duffy Publish Date April 11, 2019
FDA: Opioid Med Labels Will Include More Info on Appropriate Tapering in Physically Dependent Patients By Steve Duffy Publish Date April 10, 2019
FDA Warns Against the Use of Previously-Owned, Unauthorized Test Strips By Steve Duffy Publish Date April 9, 2019
FDA Cracks Down on Companies Selling E-Liquids Resembling Prescription Cough Meds By Steve Duffy Publish Date April 5, 2019
