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: Nimbus: Administration Set, Flex, PainPro, also known as the Halo Ambulatory Infusion System Nimbus II: PainPRO, Flex, Plus, EpiD, and EMS Product Codes: See Recall…

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 Name: Stay-Safe Catheter Extension Sets, Stay-Safe/Luer Lock Adapter Product Codes: See Recall Database Entries: Devices Recalled in the U.S.: 2,192,535  Dates Distributed: March 5, 2003 to…

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: Disposable Biopsy Needles (911933) Product Codes: HAW Lot Number: 837838839 Distribution Dates: August 29, 2023 to January 5, 2024 Devices Recalled in the U.S.: 10…

Please be aware, this recall is a correction, not a product removal. 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 Name: Perseus A500 Product Codes: See Recall Database Entry Devices Recalled in the U.S.:…

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: GeoMed Custom Tracecarts Product Codes: LRO Model Numbers: 53-1829 Laminectomy Tracecart 53-1831 Ortho Total Joint Tracecart 53-1836 General Surgery Tracecart Distribution Dates: August 25, 2022…

Summary Company Announcement Date: April 23, 2024 FDA Publish Date: April 23, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Decreased Potency Company Name: Dr. Reddy’s Laboratories Inc Brand Name: Brand Name(s) Dr. Reddy’s Product Description: Product Description Sapropterin Dihydrochloride Powder for Oral Solution 100 mg Company Announcement FOR IMMEDIATE RELEASE Hyderabad India…

Date Issued: April 22, 2024 The U.S. Food and Drug Administration (FDA) encourages the public to follow established choking rescue protocols, which are step-by-step guides, approved by the American Red Cross and the American Heart Association to relieve the airway obstruction in choking victims. These rescue protocols include abdominal thrusts (also called the “Heimlich” maneuver)…

Please be aware, this recall is a correction, not a product removal. 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: LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0. Product Codes: FRN…

Please be aware, this recall is a correction, not a product removal. 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 Name: Obsidio Conformable Embolic Product Codes: See Medical Device Recall Database Entry  Distribution Dates:…

Please be aware, this recall is a correction, not a product removal. 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: HeartMate II and HeartMate 3 Left Ventricular Assist System (LVAS) Product Codes: DSQ…