Medical Prosthesis Recalls

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Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls

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 problems or death.

Risk of Device Breaking in Patients with STAR Ankle …

https://www.fda.gov/medical-devices/safety-communications/risk-device-component-breaking-patients-strykers-star-ankle-fda-safety-communication

The STAR Ankle is indicated for use as a non-cemented total ankle prosthetic (“artificial joint”) and used to replace a painful arthritic ankle joint due to osteoarthritis, …

Implants and Prosthetics | FDA

https://www.fda.gov/medical-devices/products-and-medical-procedures/implants-and-prosthetics

Medical implants are devices or tissues that are placed inside or on the surface of the body. Many implants are prosthetics, intended to replace missing body parts. Other implants …

Teleflex Incorporated Announces Worldwide Recall of …

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teleflex-incorporated-announces-worldwide-recall-arrow-trerotolatm-over-wire-ptdr-kit-percutaneous

Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and surgery, has announced a worldwide recall of Arrow …

Knee Replacement Lawsuits | 2022 Exactech Recall Info …

https://www.consumersafety.org/medical-device-lawsuits/knee-replacement/

The U.S. Food and Drug Administration keeps a recall database for medical devices. According to the agency's database, there were nearly 1,300 recalls on knee replacement systems or components …

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 …

Knee Replacement Recalls | Stryker, Zimmer & DePuy …

https://www.drugwatch.com/knee-replacement/recalls/

Nearly 1,000 implant parts used in knee surgeries have been affected by DePuy, Zimmer-Biomet and Stryker knee replacement recalls. Lawsuits blame manufacturers for selling defective devices. The advocacy group …

Hip Replacement Recall | Causes and FDA Information

https://www.drugwatch.com/hip-replacement/recalls/

From 2002 to 2013, Consumer’s Union found 578 hip replacement recalls from Biomet, DePuy, Smith & Nephew, Stryker, Wright and Zimmer. Causes for hip implant recalls include design flaws, early implant failure and …

GE HealthCare Recalls Nuclear Medicine 600/800 …

https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

See Medical Device Recall Database entry for more information. Distribution Dates: April 1, 2018 to December 16, 2022; Devices Recalled in the U.S.: 688; Date …

Reverse Shoulder Replacement Lawsuits | Recall …

https://www.drugwatch.com/reverse-shoulder-replacement/lawsuits/

In December 2016, Zimmer Biomet recalled 3,662 reverse shoulder components of its Comprehensive model line. It was one of the largest recalls of reverse shoulder devices in recent years. In the recall notice, …

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