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Cordis Recalls SUPER TORQUE MB Angiographic Catheter with Radiopaque Marker Bands Due to Potential for Marker Bands to Move or Dislodge

Murilo Freitas - 04:00, 21 de septiembre de 2021458
This catheter is used to visualize and measure parts of the vascular system when used with radiopaque (X-ray detectable) contrast media.

http://www.fda.gov/medical-devices/medical-device-recalls/cordis-recalls-super-torque-mb-angiographic-catheter-radiopaque-marker-bands-due-potential-marker

 
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Medtronic Recalls Pipeline Flex Embolization Devices for Risk of Delivery System Fractures During Placement, Retrieval, or Movement of Device

Murilo Freitas - 04:00, 21 de septiembre de 2021443
Pipeline Flex Embolization Devices are intended to treat wide-neck and fusiform brain aneurysms. Pieces of the delivery system may break off while in use.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-pipeline-flex-embolization-devices-risk-delivery-system-fractures-during-placement

 
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IntegraDose Compounding Services, LLC Issues Voluntary Nationwide Recall of Cefazolin Injection Products Due to a Lack of Sterility Assurance

Murilo Freitas - 04:00, 20 de septiembre de 2021434
Minneapolis, Minnesota, IntegraDose Compounding Services is voluntarily recalling nine lots, listed in the table below, of cefazolin 2 gram in 20 mL syringe for injection and two lots of cefazolin 3 gram in 100 mL 0.9% sodium chloride bag for injection due to a lack of sterility assurance resulting

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/integradose-compounding-services-llc-issues-voluntary-nationwide-recall-cefazolin-injection-products

 
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