Recalls on knee replacement devices
Webb7 apr. 2024 · Exactech Knee Devices Recalled. On August 30, 2024, Exactech, a medical device company, initiated a Class 2 recall of certain lots of their OPTETRAK, OPTETRAK … WebbYou can find out about specific knee replacement recalls by: Searching the Food and Drug Administration (FDA) website. The FDA maintains a medical device recall database. You …
Recalls on knee replacement devices
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Webb5 dec. 2024 · Several medical device manufacturers design and manufacture knee replacement systems and some have proven to be more successful than others. DePuy … Webb5 apr. 2024 · Recalled Exactech knee and ankle implant replacements include: Optetrak (released in 1994) Optetrak Logic (released in 2009) Truliant (released in 2024) Vantage (released in 2016) To find out if your knee replacement is included in the recall, contact your doctor or orthopedic surgeon for detailed medical records.
Webb9 aug. 2024 · 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. … Webbför 17 timmar sedan · Philips clarified on Friday that 2.2 million devices it has repaired or replaced in a major recall of respiratory devices are actually in the hands of patients in the United States.
WebbExactech has issued massive recalls for some of its knee, ankle, and hip replacement devices. Exactech Knee and Ankle UHMWPE Inserts On February 7, 2024, Exactech sent an Urgent Medical Device Correction notice to knee and ankle surgeons, hospitals, and healthcare professionals. Webb30 mars 2024 · According to data from the USFDA (United States Food and Drug Administration), 709 knee replacement implants have been recalled by six renowned manufacturers between February 2003 and May 2013, with DePuy and Zimmer scoring the highest among others.
Webb6 juni 2024 · Metal on plastic. This is the most common type of implant. It features a metal femoral component that rides on a polyethylene plastic spacer attached to the tibial component. The metals commonly used include cobalt-chromium, titanium, zirconium, and nickel. Metal-on-plastic is the least expensive type of implant and has the longest track …
WebbThe FDA went so far as to issue a recall, affecting the nearly 12,000 artificial knees implanted in patients and warning doctors to clear their shelves of Zimmer Persona knees. The Persona was introduced as a more “personalized” knee replacement, designed to act more like a natural human knee. dafi filmWebb26 jan. 2024 · Smith & Nephew Knee Implants Oxinium Pro-Fix II and the Oxinium Genesis II In August 2003, the London-based medical device manufacturer Smith & Nephew recalled of two of their knee... dafi alkaline pitcherWebbSmith & Nephew issued 11 Class II recalls. The devices/tools were recalled because of: • Packaging issues: the sterility of tools used in knee replacement procedure may be compromised; devices “mispackaged” • Labeling issues: Markings for the drill guide are on the wrong side Stryker Stryker recalled 118 devices/components. dafi company limitedWebb6 juni 2024 · Metal on plastic. This is the most common type of implant. It features a metal femoral component that rides on a polyethylene plastic spacer attached to the tibial … dafi for promotionsWebb7 okt. 2024 · A recalled knee replacement system has kicked off new product liability litigation in Georgia after a recipient alleged portions of the medical device “sheared” inside his knee. And it’s... dafi bottleWebb17 juni 2024 · 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. Are there any recalls on Zimmer knee replacements? Zimmer Knee Replacement Recall. dafi flascheWebbThe recall affected 3475 units of the knee replacement device. Patient complaints registered as adverse events with the FDA prompted the agency to investigate the … dafi salud comas