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Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
- The FDA posts summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health...
2021 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2021-medical-device-recalls
- Dec 16, 2021
Breast Implant Recall: What You Need to Know
- https://www.cancer.org/latest-news/breast-implant-recall-what-you-need-to-know.html
- What to do if you have a recalled implant If you already have breast implants, the FDA advises you to continue your regular, routine medical care and follow-up. If you …
Medical Device Recalls - Food and Drug Administration
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm
What Do Clinicians and Organizations Owe Patients …
- https://journalofethics.ama-assn.org/article/what-do-clinicians-and-organizations-owe-patients-recalled-implanted-devices-or-materials/2021-09
Seven serious medical device failures that have led to …
- https://www.nsmedicaldevices.com/analysis/medical-device-failures-fda-recalls/
- We take a look at seven medical devices that have been hit with Class I FDA recalls in the past few years. Seven serious medical device failures 1. Allergan breast implants In July 2019, US pharma and …
Allergan Breast Implant Recalls | List of Affected Models
- https://www.drugwatch.com/allergan-breast-implants/recalls/
- Allergan Breast Implant Recalls. In July 2019, the FDA requested that Allergan recall its Biocell textured breast implants because they had been linked to BIA-ALCL, or breast implant-associated anaplastic large …
Exactech Recall Information | Surgeons and Patients
- https://www.exac.com/medical-professionals/recall-information/
- Exactech is committed to addressing recall-related out-of-pocket expenses, and has partnered with Broadspire, a Third-Party Administrator, to manage the claims …
Hip Replacement Lawsuit | 2020 Recalls & Settlements
- https://www.consumersafety.org/medical-device-lawsuits/hip-replacement/
- In August 2016, Stryker issued a voluntary recall on more than 42,500 of its Stryker LFIT V40 femoral heads - the part of the hip implant that attaches to the thigh bone. According to the FDA medical …
Implant Device Recalls - American Academy of …
- https://www.aaos.org/globalassets/about/bylaws-library/information-statements/1019-implant-device-recalls1.pdf
- 1. be aware of device recalls and potential health problems associated withthem; 2. report incidents of adverse events related to medical products via MedWatch (online at …
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