Titanium Knee Replacement Recall. Click the links below to see if your implant is affected by a recall. at least 200,000 exactech knee, hip and ankle devices have been recalled since 2021. the aaos device recall dashboard provides orthopaedic surgeons with timely recall information that will protect the health and. us exactech recall information. This is an informational page for patients to learn facts about a specific recall and find out if an implant that was packaged in nonconforming packaging was used during your procedure. on february 8, 2022, exactech, inc., an orthopedic device company headquartered in gainesville, florida, usa, issued a recall of implant components used in several of its knee and ankle systems, related to exactech’s packaging process. knee replacement recalls have been issued because of loosening, early wear or faulty packaging. Lawsuits blame manufacturers for selling defective devices. A landmark 2013 consumers union report identified 709 knee implant device or component recalls. by february 2022, the manufacturer expanded a voluntary recall for certain knee replacements and total ankle. Nearly 1,000 implant parts used in knee surgeries have been affected by depuy, zimmer biomet and stryker knee replacement recalls. the four largest knee implant manufacturers and wright medical issued nearly 800 recalls between 2003 and 2019.
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us exactech recall information. This is an informational page for patients to learn facts about a specific recall and find out if an implant that was packaged in nonconforming packaging was used during your procedure. knee replacement recalls have been issued because of loosening, early wear or faulty packaging. Nearly 1,000 implant parts used in knee surgeries have been affected by depuy, zimmer biomet and stryker knee replacement recalls. by february 2022, the manufacturer expanded a voluntary recall for certain knee replacements and total ankle. the aaos device recall dashboard provides orthopaedic surgeons with timely recall information that will protect the health and. Click the links below to see if your implant is affected by a recall. on february 8, 2022, exactech, inc., an orthopedic device company headquartered in gainesville, florida, usa, issued a recall of implant components used in several of its knee and ankle systems, related to exactech’s packaging process. Lawsuits blame manufacturers for selling defective devices. the four largest knee implant manufacturers and wright medical issued nearly 800 recalls between 2003 and 2019.
How Do I Know if My Knee Replacement Has Been Recalled? Free Case Review
Titanium Knee Replacement Recall knee replacement recalls have been issued because of loosening, early wear or faulty packaging. us exactech recall information. Nearly 1,000 implant parts used in knee surgeries have been affected by depuy, zimmer biomet and stryker knee replacement recalls. by february 2022, the manufacturer expanded a voluntary recall for certain knee replacements and total ankle. on february 8, 2022, exactech, inc., an orthopedic device company headquartered in gainesville, florida, usa, issued a recall of implant components used in several of its knee and ankle systems, related to exactech’s packaging process. Lawsuits blame manufacturers for selling defective devices. the four largest knee implant manufacturers and wright medical issued nearly 800 recalls between 2003 and 2019. A landmark 2013 consumers union report identified 709 knee implant device or component recalls. the aaos device recall dashboard provides orthopaedic surgeons with timely recall information that will protect the health and. This is an informational page for patients to learn facts about a specific recall and find out if an implant that was packaged in nonconforming packaging was used during your procedure. at least 200,000 exactech knee, hip and ankle devices have been recalled since 2021. knee replacement recalls have been issued because of loosening, early wear or faulty packaging. Click the links below to see if your implant is affected by a recall.
