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1. www.accessdata.fda.gov › scripts › cdrhClass 2 Device Recall Smith & Nephew BIRMINGHAM HIP (TM)...

   www.accessdata.fda.gov › scripts › cdrh

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   3 cze 2015 · for Recall: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had revision rates which were higher than established benchmarks. FDA Determined Cause 2: Device Design: Action:...

   • Class 2 Device Recall Birmingham Hip Resurfacing Femoral Head

     The firm initiated the recall by email and letter on...

2. www.fda.gov › medical-devices › safety-communicationsDo Not Use Synovo Total Hip Resurfacing System: FDA Safety ...

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   3 sty 2024 · The safety and effectiveness of the Synovo Total Hip System, including the Femoral Resurfacing Cup, Acetabular Fixation Cup, and the Acetabular Bearing, have not been established. The Synovo...

3. www.tga.gov.au › safety › recall-actionsBirmingham Hip Modular Head (used in hip replacements)

   www.tga.gov.au › safety › recall-actions

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   Smith & Nephew has issued a hazard alert to implanting surgeons who have previously used the component. The BHMH is no longer available for primary hip replacement surgery.

4. www.drugwatch.com › hip-replacement › smith-nephewSmith & Nephew Hip Replacement Lawsuits: Hip Recall Updates -...

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   1 paź 2024 · People have filed Smith & Nephew hip replacement lawsuits because the manufacturer’s metal-on-metal devices led to metallosis and other serious complications. Smith & Nephew recalled 4,000 R3 Acetabular Hip Systems in 2012 and 2,000 Modular SMF and Modular Redapt Revision Femoral Hip Systems in 2016 over issues that could result in more lawsuits.

5. www.consumersafety.org › medical-device-lawsuits › hip-replacementHip Replacement Lawsuit | 2020 Recalls & Settlements -...

   www.consumersafety.org › medical-device-lawsuits › hip-replacement

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   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

6. www.accessdata.fda.gov › scripts › cdrhClass 2 Device Recall Birmingham Hip Resurfacing Femoral Head

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   11 maj 2018 · The firm initiated the recall by email and letter on 05/11/2018. Consignees are asked to inspect inventory, locate and quarantine affected, unused devices. Affected product will be returned to...

7. www.verywellhealth.com › birmingham-hip-resurfacing-system-189866How the Birmingham Hip Resurfacing System Works - Verywell Health

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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.