{"id":2958,"date":"2024-11-19T08:00:45","date_gmt":"2024-11-19T08:00:45","guid":{"rendered":"https:\/\/www.groupactionlawyers.co.uk\/blog\/?p=2958"},"modified":"2024-10-09T14:04:11","modified_gmt":"2024-10-09T13:04:11","slug":"cpt-hip-system-femoral-stem-mhra-matter","status":"publish","type":"post","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/cpt-hip-system-femoral-stem-mhra-matter","title":{"rendered":"CPT Hip System Femoral Stem MHRA Matter"},"content":{"rendered":"<p>If you have experienced complications following surgery involving the CPT Hip System Femoral Stem, the matter was recently highlighted in a recent MHRA alert.<\/p>\n<p>Patients with this medical device potentially face some risks, and The Group Action Lawyers are assessing the situation.<\/p>\n<p><!--more--><\/p>\n<h3><strong>What is the CPT Hip System Femoral Stem?<\/strong><\/h3>\n<p>The CPT Hip System Femoral Stem is understood to be a medical implant used in hip replacement surgeries, designed to offer patients improved mobility and reduced pain. It is understood to work by replacing the damaged or deteriorated hip joint, providing an artificial alternative to help restore function. However, a recent <a href=\"https:\/\/www.gov.uk\/drug-device-alerts\/cpt-hip-system-femoral-stem-12-slash-14-neck-taper-increased-risk-of-postoperative-periprosthetic-femoral-fracture-dsi-slash-2024-slash-007?utm_medium=email&amp;utm_campaign=govuk-notifications-topic&amp;utm_source=320f30bf-d2d4-481a-8a03-256db7d3eb76&amp;utm_content=immediately\" target=\"_blank\" rel=\"noopener\"><strong>safety alert issued<\/strong><\/a> by the Medicines and Healthcare products Regulatory Agency (MHRA) has raised concerns over this specific implant.<\/p>\n<p>The MHRA reportedly found that patients who received the device with a 12\/14 neck taper could reportedly face an increased risk of postoperative periprosthetic femoral fractures. This means that, following surgery, patients may be at greater risk of suffering fractures around the implanted femoral stem, potentially leading to complications, further surgeries, or extended recovery periods.<\/p>\n<p>If you or a loved one have been affected by this, you may be eligible to pursue compensation. At The Group Action Lawyers, we can help patients to make claims as part of a group action lawsuit for such matters, holding manufacturers accountable for any proven physical, emotional, and financial harm caused.<\/p>\n<h3><strong>Understanding the Risk and Your Rights<\/strong><\/h3>\n<p>Receiving the CPT Hip System Femoral Stem implant and experiencing postoperative complications, such as a femoral fracture, could result in significant pain, limited mobility, and the need for additional surgeries. For many patients, the complications potentially caused by this implant could impact their quality of life and long-term health. The MHRA alert confirms the increased risk of femoral fractures due to the 12\/14 neck taper in the CPT Hip System Femoral Stem.<\/p>\n<p>Patients suffering from postoperative complications as a result of this defective device may face:<\/p>\n<p>Additional Surgeries: To correct fractures or remove the defective implant, you may require one or more revision surgeries, which can be invasive and painful.<\/p>\n<p>Extended Recovery Periods: Additional surgeries or complications can prolong recovery, limiting mobility and affecting daily life.<\/p>\n<p>Financial Strain: Medical bills, physiotherapy, and time off work due to complications can put a financial burden on patients and their families.<\/p>\n<p>Emotional Distress: The stress and anxiety of facing more surgeries or living with ongoing pain can lead to mental and emotional strain.<\/p>\n<h3><strong>The Group Action Lawyers and What We Do<\/strong><\/h3>\n<p>For issues of this nature, <a href=\"https:\/\/www.groupactionlawyers.co.uk\/contact\" target=\"_blank\" rel=\"noopener\"><strong>contact us to discuss your case<\/strong><\/a>. We can assess whether your situation fits within the criteria of a group action claim.<\/p>\n<p>We can work with you to gather all necessary medical records and documentation, and any complications or surgeries you have undergone as a result.\u00a0 At The Group Action Lawyers, we can operate on a no-win, no-fee basis.<\/p>\n<p>If you or a loved one have suffered from complications due to issues such as the CPT Hip System Femoral Stem matter, do not delay in seeking justice. <a href=\"https:\/\/www.groupactionlawyers.co.uk\/contact\" target=\"_blank\" rel=\"noopener\"><strong>Contact The Group Action Lawyers today to discuss your claim and join the group action<\/strong>.<\/a><\/p>\n<p>Our team is committed to ensuring that those affected by proven defective medical devices can receive the compensation they deserve.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>If you have experienced complications following surgery involving the CPT Hip System Femoral Stem, the matter was recently highlighted in a recent MHRA alert. Patients with this medical device potentially face some risks, and The Group Action Lawyers are assessing the situation.<\/p>\n","protected":false},"author":1,"featured_media":2959,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[80,36,23,1,27,10],"tags":[16,58,54,68,60,61,20,11,55,8],"class_list":["post-2958","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-group-actions","category-health","category-industrial","category-latest","category-products","category-recalls","tag-investigations","tag-medical-devices","tag-medical-implants","tag-medical-negligence","tag-medical-product","tag-medical-recall","tag-mhra","tag-news","tag-product-safety","tag-recalls"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - 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Steril Milano is understood to provide services for sterilising medical equipment\u2026","rel":"","context":"In &quot;Group Actions&quot;","block_context":{"text":"Group Actions","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/group-actions"},"img":{"alt_text":"hip replacement claims","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/hip-replacement-claims-min.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/hip-replacement-claims-min.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/hip-replacement-claims-min.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/hip-replacement-claims-min.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":1054,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/depuy-synthes-impactor-pfna-blade-recalled-over-risk-infection","url_meta":{"origin":2958,"position":2},"title":"DePuy Synthes Impactor for PFNA blade recalled over risk of infection","author":"Admin","date":"1st November 2017","format":false,"excerpt":"Manufactured by Synthes, the DePuy impactors used for Proximal Femoral Nail Antirotation (PFNA) have been recalled over potentially dangerous risks of infection. PFNA's are metal devices inserted into the femur bone to strengthen it. The U.K.'s Medicines and Healthcare Products Regulation Agency (MHRA) has noted a defect with the medical\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"elbow implants recall","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/elbow-implants-recall-min.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/elbow-implants-recall-min.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/elbow-implants-recall-min.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/elbow-implants-recall-min.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":1754,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/elbow-implant-problems-and-stryker-recall","url_meta":{"origin":2958,"position":3},"title":"Elbow implant problems and Stryker recall","author":"Author","date":"1st April 2019","format":false,"excerpt":"If you\u2019re suffering with elbow implant problems, you may want to read this. The recent Stryker recall could be linked to any complications you\u2019re experiencing. Back in November 2017, a Field Safety Notice was filed for a recall of the rHead Radial Head and the Uni-Elbow prosthesis. In February this\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"medical device alert","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2017\/04\/medical-device-alert.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2017\/04\/medical-device-alert.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2017\/04\/medical-device-alert.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2017\/04\/medical-device-alert.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":828,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/mom-hip-replacements-potentially-causing-long-lasting-injuries","url_meta":{"origin":2958,"position":4},"title":"MoM hip replacements potentially causing long-lasting injuries","author":"Admin","date":"19th July 2017","format":false,"excerpt":"All Metal-on-Metal (MoM) hip replacement patients are being recalled for advice and investigation in the U.K. The Medicines and Healthcare products Regulatory Agency (MHRA) has recently issued an updated medical device alert on 29th June 2017. It's estimated that 49,000 patients in the U.K. were given the MoM implants (with\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"mom hip implant-concerns","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/mom-hip-implant-concerns-min.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/mom-hip-implant-concerns-min.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/mom-hip-implant-concerns-min.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/mom-hip-implant-concerns-min.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":800,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/depuy-synthes-elbow-implants-mhra-recall","url_meta":{"origin":2958,"position":5},"title":"DePuy Synthes elbow implants recalled by the MHRA","author":"Admin","date":"10th July 2017","format":false,"excerpt":"The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a recall for radial head elbow artificial replacements amidst concerns over post-operative loosening of the device. Manufactured by DePuy company Synthes, the implants are suspected to loosen at the stem of the implant where it joins the bone. 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