Pipeline and approval signals
Search agency notices, approvals, recalls, and regulatory updates from global authorities.
1,099 of 1,099 tracked regulatory updates from 40 agencies and publishers, page 13 of 22.
La AEMPS informa de un posible fallo en la fijaci贸n interna de la bater铆a en determinados dispositivos de comunicaci贸n aumentativa y alternativa TD Navio Midi y TD Navio MaxiAEMPS (Spain)La AEMPS informa de un posible defecto de fabricaci贸n en la sonda intermitente uretral hidrof铆lica OnliAEMPS (Spain)La AEMPS publica una gu铆a para facilitar la solicitud de los registros simplificados especiales para medicamentos veterinariosAEMPS (Spain)Early Alert: Compact Medical Removes and Updates Use Instructions for ButterflyBVM Bag-Valve-Mask ResuscitatorsFDA MedWatchWithdrawn and Expired Guidances | DrugsFDA Drug Safety CommunicationsFDA Advises Consumers Not to Buy or Serve Once Upon a Farm Tractor Wheels Organic Toddler Soft-Baked BarsFDA MedWatchEarly Alert: B. Braun Medical Inc. Removes Streamline Bloodline Set for Dialog+FDA MedWatchMenopausal Hormone Therapies with Updated Prescribing InformationFDA Drug Safety CommunicationsPlatelet Factor 4 (PF4) Radioimmunoassay Recall: Instrumentation Laboratories Removes HemosIL AcuStar HIT-IgG(PF4-H)FDA MedWatchHospital Glucose Meter Correction: Nova Biomedical Updates Use Instructions for StatStrip Glucose Hospital Meter SystemsFDA MedWatchDrug label update: ProsaceaopenFDA Drug LabelsDrug label update: Fungicure Anti-Fungal WashopenFDA Drug LabelsEarly Alert: Medline Removes or Corrects All Medline Brand Beds and AccessoriesFDA MedWatchDrug recall: LEVOXYLopenFDA Drug RecallsDrug recall: Brush Buddies, Mint Chocolate Chip Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-520-35, Item # 88520, UPC 8 10147 88520 6openFDA Drug RecallsDrug recall: Testosterone Cypionate, 200 mg/mL, packaged in a) 5 mL vials (NDC 73271-1225-1) and b) 30 m vials ( NDC 73271-1226-2) This Is A Compounded Dug, Intramuscular Use, Office Use Only, 8400 Esters Blvd, STE 190, Irving, TX 75063.openFDA Drug RecallsDrug recall: CINACALCETopenFDA Drug RecallsDrug recall: ARGATROBANopenFDA Drug RecallsDrug recall: AMITRIPTYLINE HYDROCHLORIDEopenFDA Drug RecallsDrug recall: AMLODIPINE AND OLMESARTAN MEDOXOMILopenFDA Drug RecallsDrug recall: HEPARIN SODIUMopenFDA Drug RecallsDrug recall: TELMISARTAN AND AMLODIPINEopenFDA Drug RecallsDrug recall: ABIRTEGAopenFDA Drug RecallsDrug recall: Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL multi-dose vial, Rx only, Subcutaneous Only, Greenwich Rx.openFDA Drug RecallsDevice recall: MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64155B.openFDA Device RecallsDevice recall: InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030openFDA Device RecallsDevice recall: Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (Android) Software Version: Software version 1.2.1 Product Description: The MiniMed Go app for iOS or MiniMed Go app for Android is compatible with the following components: " SimpopenFDA Device RecallsDevice recall: Direxion Torqueable Microcatheter, NGMC/SINGLE/021/SWAN/1RO/105; Material Number: M001195290openFDA Device RecallsDevice recall: Medtronic Biopsy Needle Kit, REF: 9733068, Passive, Sterile EO, RxonlyopenFDA Device RecallsDevice recall: Ion Torrent Genexus Dx with software, Catalog: A40003539, which supports the Ion Torrent Genexus Dx Integrated SequenceropenFDA Device RecallsDevice recall: ROTOR ASSY-SW40, Reference Number 331302, when the rotors are installed in the following centrifuges: Optima XPN-100 (Model Numbers A99846 and A94469), Optima XPN-90 (Model Numbers A99842 and A94468), Optima XPN-80 (Model Numbers A99839 and A95765), Optima XE-100 (Model Numbers A99836openFDA Device RecallsDevice recall: Think Surgical Square Driver REF: 109126openFDA Device RecallsDevice recall: VOCSN (Japan) Model Number: PRT-01100-100, Package PN:PRT-01126-100. used for ventilatory support.openFDA Device RecallsDevice recall: CareLink Clinic, REF: MMT-7350openFDA Device RecallsDevice recall: Techno-Path Multichem AE Unassayed Level 2 REF: AE622XopenFDA Device RecallsDevice recall: Brand Name: VACUETTE Product Name: LH Lithium Heparin Separator Model/Catalog Number: 454008P Product Description: Greiner VACUETTE Blood Collection Tube with Lithium Heparin and Gel Separator (13 x 75 mm, 3.5ml)openFDA Device RecallsEarly Alert: B. Braun Removes Streamline Bloodline Set for Dialog+FDA MedWatchDrug label update: HEB Cherry Cough DropsopenFDA Drug LabelsDrug label update: BM ColocynthisopenFDA Drug LabelsDrug label update: OxcarbazepineopenFDA Drug LabelsDrug label update: CarbamazepineopenFDA Drug LabelsDrug label update: Sertraline HClopenFDA Drug LabelsDrug label update: LAXATIVEopenFDA Drug LabelsDrug label update: CVS Diphenhydramine HydrochlorideopenFDA Drug LabelsDrug Alerts and StatementsFDA Drug Safety CommunicationsWedgewood Pharmacy Issues Recall of Certain Compounded Veterinary Medications Within Expiry Due to Potential Potency IssuesFDA MedWatchDrug recall: Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032.openFDA Drug RecallsDrug recall: HYDROCORTISONE SODIUM SUCCINATEopenFDA Drug RecallsDrug recall: METOCLOPRAMIDEopenFDA Drug RecallsDevice recall: Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395AopenFDA Device Recalls