Summary Company Announcement Date: August 30, 2023 FDA Publish Date: August 31, 2023 Product Type: Drugs Reason for Announcement: Recall Reason Description Label Mix-Up Company Name: Marlex Pharmaceuticals, Inc. Brand Name: Brand Name(s) Marlex Pharmaceuticals, Inc. Product Description: Product Description Digoxin Tablets USP, 0.125mg and 0.25mg Company Announcement FOR IMMEDIATE RELEASE – August 30, 2023…
Getinge/Maquet/Datascope Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for Gas Loss and Gas Gain Failures
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 Product Names: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Product Codes and Models: Distribution Dates: March 6, 2012 to May 19,…
Getinge/Maquet/Datascope Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for Power Failures When Device is Unseated from Cart
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 Recalled Product: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Product Models: Distribution Dates: March 6, 2012 to May 19, 2023 Devices…
Universal Meditech Inc. Issues Nationwide Recall of All Products Manufactured Between March 2021 and November 2022
Summary Company Announcement Date: August 28, 2023 FDA Publish Date: August 31, 2023 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Due to lack of appropriate premarket clearance or approval which potentially could result in inaccurate test results Company Name: Universal Meditech Inc. Brand Name: Brand Name(s) Healthy Wiser and more Product Description:…
Norfolk Man Charged with Price Gouging N95 Masks in Early Months of COVID-19 Pandemic
Department of JusticeU.S. Attorney’s OfficeDistrict of Massachusetts FOR IMMEDIATE RELEASEThursday, August 31, 2023 Defendant allegedly conspired to sell tens of thousands of masks at excessive markups BOSTON – A Norfolk, Mass. man has been charged and has agreed to plead guilty to conspiring to price gouge hospitals for scarce N95 filtering facepiece respirators (N95 masks)…
Weis Markets Issues an Allergy Alert for Weis Quality Premium Brownie Moose Tracks Ice Cream Due to Undeclared Egg Allergen
Summary Company Announcement Date: August 31, 2023 FDA Publish Date: August 31, 2023 Product Type: Food & Beverages Ice Cream/Frozen Dairy Allergens Reason for Announcement: Recall Reason Description Undeclared egg Company Name: Weis Markets Inc. Brand Name: Brand Name(s) Weis Quality Product Description: Product Description Brownie Moose Tracks Ice Cream Company Announcement Sunbury, PA (AUGUST…
Getinge/Maquet/Datascope Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for Autofill Failure Alarms Resulting in Pump Stops
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 Recalled Product: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Product Models: Distribution Dates: March 6, 2012 to May 19, 2023 Devices…
The Ice Cream House is Voluntarily Recalling All Dairy Ice Cream Products and Non-Dairy [Parve] Frozen Dessert Products Due to Potential Health Risk in Regards to Listeria Monocytogenes
Summary Company Announcement Date: August 30, 2023 FDA Publish Date: August 30, 2023 Product Type: Food & Beverages Ice Cream/Frozen Dairy Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: Ice Cream House Brand Name: Brand Name(s) Ice Cream House Product Description: Product Description Dairy and Non-Dairy…
TODORGANIC INC. Recalls Nuez De La India Seeds Product Due to Possible Health Risk
Summary Company Announcement Date: August 30, 2023 FDA Publish Date: August 30, 2023 Product Type: Food & Beverages Seeds Reason for Announcement: Recall Reason Description Possible Health Risk-Contain cardiac glycosides Company Name: Todorganic, Inc. Brand Name: Brand Name(s) Todorganic Natural Products Product Description: Product Description Nuez De La India Seeds Company Announcement TODORGANIC INC Middleburg…
TODORGANIC INC Retira Del Mercado Producto De Nuez De La India Seeds Debido a Posible Riesgo Para La Salud
Summary Company Announcement Date: August 30, 2023 FDA Publish Date: August 30, 2023 Product Type: Food & Beverages Seeds Reason for Announcement: Recall Reason Description Possible Health Risk-Contain cardiac glycosides Company Name: Todorganic, Inc. Brand Name: Brand Name(s) Todorganic Natural Products Product Description: Product Description Nuez De La India Seeds Company Announcement TODORGANIC INC Middleburg…