On October 2, 2025, Glenmark Pharmaceuticals Europe Ltd announced a precautionary recall of a specific batch…
Category: Europe
europe updates on medical device regulation and quality.
Tamoxifen 20mg Tablets Recall: Stability Testing Uncovers Dissolution Issue
Wockhardt UK Limited issued a precautionary recall of a batch of Tamoxifen 20mg film-coated tablets after…
Urgent Notification: Superseded Patient Information in Erythromycin Stearate BP 250mg Tablet Batch
Amdipharm UK Ltd has reported a critical issue regarding a batch of Erythromycin Stearate BP 250mg…
Critical Advisory: New Aurum 10ml CONNECT Syringe Barrel Requires Compatible Needle-Free Connectors to Prevent Blockages
Healthcare professionals are urged to adopt compatible needle-free connectors (NFCs) with the newly phased-in Aurum 10ml…
Critical Update: Barcode Error Identified in Simvastatin 10mg From Crescent Pharma
Crescent Pharma Limited has reported a significant issue related to one of its distributed products, Simvastatin…
Zaditen Eye Drops Recall Announced Over Microbial Contamination Risks
In a recent update concerning pharmaceutical safety, Thea Pharmaceuticals Limited (trading as Laboratoires Théa) initiated a…
Critical Updates: Field Safety Notices Released for 30 June to 4 July 2025
Healthcare professionals specializing in clinical, quality, and regulatory affairs should note the latest developments regarding medical…
Critical Updates: Field Safety Notices Published for Medical Devices (7–11 July 2025)
Healthcare professionals and teams responsible for compliance and patient safety should take note of the latest…
Latest Field Safety Notices Highlight Critical Updates for Medical Devices: 14–18 July 2025
Medical device professionals should be aware of the latest Field Safety Notices (FSNs) published between 14…
Critical Update: Positive Bias Detected in Trinity Biotech Premier Hb9210™ HbA1c Analyser Results
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has issued an alert regarding the Trinity…