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Physio-Control has announced a recall of specific lots of its Quik-Combo adult pacing/defibrillation/ECG electrodes and its Red-Pak preconnected system due to possible damage to the wire insulation during the manufacturing process. Read More
Innovative Sterilization Technologies has received an FDA warning letter for failing to establish and maintain procedures when dealing with contract manufacturers. Read More
The FDA is calling on healthcare facilities to immediately implement employee training for updated reprocessing instructions for two Olympus duodenoscope models. Read More
The third time is not always the charm, as radiology clinic MRI Imaging Specialist learned the hard way following three failed FDA inspections in nearly two years, a recent FDA warning letter shows. Read More