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2021 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2021-medical-device-recalls
- Medtronic Recalls Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy (CRT-Ds) Due to Risk of Shortened ...
Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
- If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. …
Guidant recalls heart defibrillators - NBC News
- https://www.nbcnews.com/health/health-news/guidant-recalls-heart-defibrillators-flna1C9442167
- 7 models recalled Guidant came under fire this spring after The New York Times reported that it failed to alert physicians about potential problems with the Ventak Prizm 2 DR …
Class 2 Device Recall Guidant CONTAK RENEWAL 3
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=46324
- Guidant CONTAK RENEWAL 3 (models H170, H175) CONTAK RENEWAL 3 HE (models H177, H179) Cardiac Resynchronization Therapy Defibrillator (CRT-D). …
Medical Device Manufacturer Guidant Charged in Failure …
- https://www.justice.gov/opa/pr/medical-device-manufacturer-guidant-charged-failure-report-defibrillator-safety-problems-fda
- WASHINGTON – Medical device manufacturer Guidant LLC, a wholly-owned subsidiary of Boston Scientific Corporation, was charged today with criminal …
2022 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
- 11/01/22. Philips Respironics Recalls Certain Masks for BiPAP, CPAP Machines Due to Safety Issue with Magnets That May Affect Certain Medical Devices. 10/18/22. Jiangsu …
Medical Device Manufacturer Guidant Sentenced for …
- https://www.justice.gov/opa/pr/medical-device-manufacturer-guidant-sentenced-failure-report-defibrillator-safety-problems
- WASHINGTON – Guidant LLC, a wholly-owned subsidiary of Boston Scientific Corporation, was formally convicted and sentenced today in St. Paul, Minn., …
Guidant Defibrillator FAQ - FindLaw
- https://www.findlaw.com/injury/product-liability/guidant-defibrillator-faq.html
- Guidant Corporation makes defibrillators, which have been subject to a recall. In April 2006, Guidant Corporation was acquired by Boston Scientific. Q: Why …
Recall of Guidant Pacemakers, ICDs - WebMD
- https://www.webmd.com/heart-disease/news/20060627/recall-guidant-pacemakers-icds
- Five failures have been reported -- four in patients already implanted, and one during the implant operation. None of these patients died, although two pacemaker …
Medical Device Manufacturer Guidant Charged in Failure …
- https://www.prnewswire.com/news-releases/medical-device-manufacturer-guidant-charged-in-failure-to-report-defibrillator-safety-problems-to-fda-85372982.html
- WASHINGTON, Feb. 25 /PRNewswire-USNewswire/ -- Medical device manufacturer Guidant LLC, a wholly-owned subsidiary of Boston Scientific Corporation, …
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