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Houston Compounder Recalls Injectable Wellness Products Over Endotoxin Contamination

The recall forces patients to discard affected doses, highlighting gaps in oversight of customized medicines.

FDA Approves Rusfertide (Mimrylo) for Polycythemia Vera

FDA Approves Zanidatamab Regimens for First‑Line HER2‑Positive Gastroesophageal Cancer

FDA Grants Accelerated Approval to Genglycos for Glycogen Storage Disease Type Ia

FDA Grants Accelerated Approval for RP1 (Tudriqev) With Nivolumab in Advanced Melanoma

FDA Grants Accelerated Approval to Sanofi’s Tzield for Children With Stage 3 Type 1 Diabetes

FDA Approves First Glucocorticoid Receptor Blocker for Platinum-Resistant Ovarian Cancer

FDA Grants Accelerated Approval to Subcutaneous Lunsumio for Relapsed Follicular Lymphoma

MediNatura Recalls All ReBoost and ClearLife Nasal Sprays Over Contamination Risk

FDA Approves Durvalumab Added to Perioperative FLOT for Resectable Gastric and GEJ Cancer

FDA OKs RVO Use and Monthly Dosing for Regeneron’s Eylea HD

EU Medicines Panel Backs Teizeild to Delay Type 1 Diabetes Onset

FDA Approves Lurbinectedin Plus Atezolizumab for First-Line Maintenance in Extensive-Stage SCLC

Moderna’s mRNA-1010 Flu Vaccine Shows Superior Efficacy in Phase 3 Trial

Medtech Products Recalls Children's Honey Cough Syrup Over Bacterial Contamination