Summary Company Announcement Date: June 27, 2022 FDA Publish Date: June 30, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Contain Tadalafil Company Name: Loud Muscle Science, LLC Brand Name: Brand Name(s) Launch Sequence Product Description: Product Description Launch Sequence Aphrodisia and Euphoria Capsules Company Announcement FOR IMMEDIATE RELEASE – 6/27/22 – Hauppauge,…
Update: Mammography Problems at Capitol Radiology, LLC, doing business as Laurel Radiology Services in Laurel, Maryland: FDA Safety Communication
Date Issued: June 30, 2022 The U.S. Food and Drug Administration (FDA) is updating the May 2021 Safety Communication to alert the public that Capitol Radiology, LLC, doing business as Laurel Radiology Services, located in Laurel, Maryland is currently unaccredited and uncertified to perform mammography and cannot legally provide mammography services. The facility’s Mammography Quality…
A&M Farms Initiates a Recall Of Specific Little Bear Brand Whole Vidalia Onions Sold By The Pound at Retail Because of Possible Health Risk
Summary Company Announcement Date: June 30, 2022 FDA Publish Date: June 30, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: A&M Farms Brand Name: Brand Name(s) Little Bear Product Description: Product Description Whole Vidalia onions Company Announcement A&M Farms of Lyons, Georgia,…
Updated -Blount Fine Foods Voluntarily Recalls a Limited Amount (a Single Lot) of Southwest Corn Chowder Due to Undeclared Wheat Allergen
Summary Company Announcement Date: June 24, 2022 FDA Publish Date: July 01, 2022 Product Type: Food & Beverages Soup Allergens Reason for Announcement: Recall Reason Description Undeclared wheat allergen Company Name: Blount Fine Foods Brand Name: Brand Name(s) Panera at Home Product Description: Product Description Southwest Corn Chowder Company Announcement Updated – Additional Product Images…
Information Regarding Medically Necessary Specialty Infant Formulas: Notice to Health Care Providers
July 1, 2022 The U.S. Food and Drug Administration is providing information to health care professionals to help their patients obtain access to medically necessary specialty, amino acid-based and metabolic infant formula products. The FDA is continuing to work to ensure infants and individuals with medical conditions who rely on certain specialty, amino acid-based and…
Copiktra (duvelisib): Drug Safety Communication – FDA Warns about Possible Increased Risk of Death and Serious Side Effects
[Posted 06/30/2022] AUDIENCE: Patient, Health Professional, Pharmacy, Oncology ISSUE: The FDA is warning that results from a clinical trial show a possible increased risk of death with Copiktra (duvelisib) compared to another medicine to treat a chronic blood cancer called leukemia and a lymphoma, a cancer found in the lymph nodes. The trial also found Copiktra was…
Bryant Ranch Prepack Inc. Issues Voluntary Nationwide Recall of Morphine Sulfate 30 mg Extended Release and Morphine Sulfate 60 mg Extended-Release Due to Label-Mix Up
Summary Company Announcement Date: June 28, 2022 FDA Publish Date: June 29, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Incorrect labeling Company Name: Bryant Ranch Prepack Inc. Brand Name: Brand Name(s) Bryant Ranch Prepack Inc. Product Description: Product Description Morphine Sulfate 30 mg Extended-Release tablets Company Announcement 06/28/2022 – Burbank, California, Bryant…
Do Not Use Baby Neck Floats Due to the Risk of Death or Injury: FDA Safety Communication
Date Issued: June 28, 2022 The U.S. Food and Drug Administration (FDA) is warning parents, caregivers, and health care providers not to use neck floats with babies for water therapy interventions, especially with babies who have developmental delays or special needs, such as spina bifida, spinal muscular atrophy (SMA) type 1, Down syndrome, or cerebral…
Defendant Convicted of Operating Large-Scale Opioid “Pill Mill” in Queens
Department of JusticeEastern District of New York FOR IMMEDIATE RELEASEMonday, June 27, 2022 Defendant Imported Millions of Misbranded Prescription Pills from India and Shipped Them by Mail to Customers Across the United States A federal jury in Brooklyn returned a guilty verdict today against Ezhil Sezhian Kamaldoss on all counts of a superseding indictment charging him…
Generic Drugs Undergo Rigorous FDA Review
Image Maybe you’ve had this experience: You go to fill a prescription, and the pharmacist mentions there is a generic available. You’ve noticed generic drugs often cost less and wonder: How can I be sure they are as safe and effective as brand name drugs? Applying the rigorous standards set out by law, the U.S….