Summary Company Announcement Date: February 09, 2021 FDA Publish Date: February 09, 2021 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Almonds Company Name: Hickory Harvest Foods Brand Name: Brand Name(s) Product Description: Product Description Vanilla Yogurt Covered Cranberries Company Announcement Hickory Harvest Foods of Akron, OH is recalling Vanilla…
North Carolina Sport Supplement Company and Its Owner Plead Guilty to Unlawful Distribution of Steroid-like Drugs
Department of JusticeU.S. Attorney’s OfficeWestern District of Virginia FOR IMMEDIATE RELEASETuesday, November 24, 2020 ABINGDON, Virginia – A North Carolina resident, and his sport supplement company, pleaded guilty today to a felony charge relating to the introduction of unapproved new drugs into interstate commerce, Acting United States Attorney Daniel P. Bubar announced. Brian Michael Parks, 47, of…
Shenandoah Growers, Inc Issues a Limited, Voluntary Recall of Specific Imported Organic Basil Because of Potential Health Risk
Summary Company Announcement Date: February 08, 2021 FDA Publish Date: February 08, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Cyclospora contamination Company Name: Shenandoah Growers, Inc Brand Name: Brand Name(s) Simple Truth, That’s Tasty, Shenandoah Growers Product Description: Product Description Company Announcement Shenandoah Growers, Inc (Harrisonburg, VA) out of…
Ocean Beauty Seafood LLC Issues Allergy Alert on Undeclared Soy in Publix Brand Parmesan-Crusted Wild Alaskan Salmon Fillets 12 Oz. Package
Summary Company Announcement Date: February 08, 2021 FDA Publish Date: February 08, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Soy Company Name: Ocean Beauty Seafood LLC Brand Name: Brand Name(s) Product Description: Product Description Parmesan-Crusted Wild Alaskan Salmon Fillets Company Announcement Ocean Beauty Seafood LLC of Seattle, WA is…
Xeljanz, Xeljanz XR (tofacitinib): Drug Safety Communication – Initial Safety Trial Results Find Increased Risk of Serious Heart-related Problems and Cancer with Arthritis and Ulcerative Colitis Medicine
[Posted 02/04/2021] AUDIENCE: Patient, Health Professional, Pharmacy, Rheumatology, Gastroenterology, Cardiology, Oncology ISSUE: The FDA is alerting the public that preliminary results from a safety clinical trial show an increased risk of serious heart-related problems and cancer with the arthritis and ulcerative colitis medicine Xeljanz, Xeljanz XR (tofacitinib) compared to another type of medicine called tumor necrosis…
Apotex Corp. Issues Voluntary Nationwide Recall of Enoxaparin Sodium Injection, USP Due to Mislabeling of Syringe Barrel Measurement Markings
Summary Company Announcement Date: February 02, 2021 FDA Publish Date: February 03, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Packaging error resulting in incorrect dosage listed Company Name: Apotex Corp Brand Name: Brand Name(s) Apotex Corp. Product Description: Product Description Enoxaparin Sodium Injection, USP Company Announcement Apotex Corp is voluntarily recalling two…
Business Owner Found Guilty of Committing Fraud Regarding Human Clinical Research Trials
Department of JusticeU.S. Attorney’s OfficeEastern District of Washington FOR IMMEDIATE RELEASEMonday, December 25, 2019 Richland Man Found Guilty of 47 Counts in Federal Court Richland –William D. Hyslop, United States Attorney for the Eastern District of Washington, announced that Sami Anwar, 42, of Richland, WA, was found guilty late Friday of Conspiracy to Commit Wire Fraud,…
Boston Scientific Recalls EMBLEM S-ICD Subcutaneous Electrode (Model 3501) Due to Risk of Fractures
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Products EMBLEM S-ICD Subcutaneous Electrode Model Number: 3501 Manufacturing Dates: March 2016 and November 2020 Distribution Dates: June 2017 to November 2020 Devices Recalled in the U.S.: 19,919…
Israeli National Pleads Guilty to Bail Jumping
Department of JusticeU.S. Attorney’s OfficeDistrict of New Hampshire FOR IMMEDIATE RELEASEThursday, January 28, 2021 CONCORD – Boaz BenMoshe, 58, of Israel, pleaded guilty in federal court on Wednesday to bail jumping, United States Attorney Scott W. Murray announced today. According to court documents and statements made in court, in November 2006, a federal grand jury charged BenMoshe…
Penumbra’s Recall of the JET 7 Reperfusion Catheter Due to Distal Tip Damage
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Penumbra JET 7 Reperfusion Catheter with Xtra Flex Technology, also known as JET 7 Xtra Flex All Lots Model or Catalog Numbers: The FDA’s Recall Classification Database…