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11 mar 2023 · Why were Birmingham hip resurfacing systems recalled? In 2015, manufacturer Smith & Nephew voluntarily recalled femoral heads that were 46 millimeters (mm) in diameter and smaller due to a greater risk of dislocation and a need for revision surgery.
BIRMINGHAM HIP Resurfacing System. A bone conserving total hip system, ideal for the younger or more active male patient 1-3. Brochure. Driven by experience.
10 sty 2024 · Smith & Nephew BHR. The multinational medical device maker Smith & Nephew, headquartered in Great Britain, has been the subject of many different lawsuits over various allegedly defective hip replacement products, including: Birmingham Hip Resurfacing (BHR) System; Birmingham Hip Modular Head (BHMH) - phased out in 2014-2015
25 lis 2018 · Scandals involving breast implants and all-metal hips prosthetics have raised global concerns and prompted regulatory reform in the European Union.
3 cze 2015 · The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device...
1 wrz 1999 · However in June 2015, the BHR manufacturer (Smith & Nephew) issued an urgent field safety notice, with the Australian Government’s device regulatory authority issuing a recall action notification indicating that the use of the BHR was contraindicated in females and recalling femoral and acetabular head components with femoral head sizes < 50 mm .
8 gru 2020 · 2020 marks the five-year anniversary of the recall for the Birmingham Hip Resurfacing (BHR) System manufactured by the medical device company, Smith and Nephew. The BHR is a metal-on-metal hip implant that consists of the metals cobalt and chromium.
