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  2. Medical device reporting - Wikipedia

    en.wikipedia.org/wiki/Medical_device_reporting

    Medical device reporting (MDR) is the procedure for the Food and Drug Administration to get significant medical device adverse events information from manufacturers, importers and user facilities, so these issues can be detected and corrected quickly, and the same lot of that product may be recalled.

  3. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    There are also market withdrawals [2] and medical device safety alerts'. [2] Market withdrawals occur when a product has a minor violation that does not require FDA legal action. Medical device safety alerts occur when there are unreasonable safety risks associated with using a product. [1]

  4. Federal Institute for Drugs and Medical Devices - Wikipedia

    en.wikipedia.org/wiki/Federal_Institute_for...

    The Federal Institute for Drugs and Medical Devices (in German: Bundesinstitut für Arzneimittel und Medizinprodukte – BfArM) is the medical regulatory body in Germany. It operates under the Federal Ministry of Health (BMG). It is headquartered in Bonn, Germany. [1] Its president is Karl Broich. [2]

  5. FDA identifies recall of B. Braun Medical pump system ... - AOL

    www.aol.com/news/fda-identifies-recall-b-braun...

    About 10,655 devices, which were distributed between Oct. 26, 2022 and July 17, 2023, have been recalled by the company. B. Braun Medical did not immediately respond to a Reuters request for comment.

  6. Urgent Medical Device Recall Issued for Ventilator - AOL

    www.aol.com/urgent-medical-device-recall-issued...

    The recall applies to Life2000 ventilators with the product code MS01-0118 that have the attached battery charger dongle, and were distributed in the U.S. from Aug. 21, 2023 to April 2, 2024 ...

  7. US FDA identifies recall of Philips medical imaging devices ...

    www.aol.com/news/us-fda-identifies-recall...

    The health regulator said there has been one reported event of an explosion in 22 years of use and no reports of injury or death due to the devices. The devices were distributed between Jan. 1 ...

  8. MedWatch - Wikipedia

    en.wikipedia.org/wiki/MedWatch

    The MedWatch system collects reports of adverse reactions and quality problems of drugs and medical devices but also for other FDA-regulated products (such as dietary supplements, cosmetics, medical foods, and infant formulas). As of the summer of 2011, the program had received more than 40,000 adverse event reports. [1]

  9. US FDA classifies recall of J&J's electrosurgical tools as ...

    www.aol.com/news/u-fda-classifies-recall-j...

    The tools were recalled by Megadyne Medical Products, which was acquired in 2017 by Ethicon Endo-Surgery, a ... The U.S. health regulator said it had received reports of pediatric and adult ...