Zimmer biomet recalls. Sep 22, 2022 · The AAOS Device Recall Dashboard provides orth...

Zimmer biomet recalls. Sep 22, 2022 · The AAOS Device Recall Dashboard provides orthopaedic surgeons with timely recall information that will protect the health and well-being of their patients. Food & Drug Administration (FDA) issued a warning about Zimmer Biomet’s CPT Hip System implants in September 2024, following a recall initiated by the company in July. “Zimmer Biomet Holdings” refers to the parent company only. 4 PEG AUG REAMER GUIDE LEFT; PROSTHESIS, SHOULDER FDA Home Medical Devices Databases. Aug 12, 2025 · Some medics have said they first started noticing issues with a part of a knee replacement made by American medical device company Zimmer Biomet around eight years ago. Feb 10, 2026 · Zimmer Biomet Holdings, Inc. Class 2 Device Recall Zimmer Biomet FDA Home Medical Devices Databases Mar 5, 2026 · Zimmer Biomet’s faulty hip implants have led to recalls, lawsuits and stricter FDA regulations. S. Despite acknowledging the defect, the manufacturer plans to continue selling the remaining units until the end of the year. Zimmer Biomet Holdings was incorporated in Delaware in 2001. and its subsidiaries. (ZBH) Q4 2025 Earnings Call February 10, 2026 8:30 AM ESTCompany ParticipantsDavid DeMartino - Senior Vice President of History Of Zimmer Biomet History of Zimmer Biomet Zimmer Biomet is a leading global medical technology company specializing in musculoskeletal healthcare. The recall was prompted by concerns that the cobalt-chromium alloy implant is twice as likely to cause thigh bone fractures when compared to similar products made of stainless steel. May 26, 2025 · The U. ‍ Zimmer Biomet Issues a Recall for CPT Hip System On July 2, 2024, Zimmer Biomet announced a voluntary recall of its CPT Hip System Femoral Stem with a 12/14 Neck Taper. In this report, “Zimmer Biomet,” “we,” “us,” “our,” “the Company” and similar words refer collectively to Zimmer Biomet Holdings, Inc. While some failures stemmed from metal-on-metal designs, even non-MoM models like the CPT Hip System have raised safety concerns, prompting legal and medical scrutiny. Subject: URGENT MEDICAL DEVICE RECALL Zimmer Biomet is conducting a voluntary medical device recall related to the NexGen Stemmed Option Tibial Components due to the clinically and statistically significant higher overall revision rates when these tibial components are used with either the Legacy Posterior Stabilized (LPS) Flex or LPS Flex Gender Solutions Femoral (GSF) components as compared Sep 17, 2024 · The FDA is getting the word out regarding a recall effort from Zimmer Biomet, related to its discontinued CPT hip implant and its potential link to fractures of the thigh bone after placement. Its journey through the annals of medical innovation epitomizes the evolution of orthopedic care, driven by a commitment to improve patients' quality of life. MAUDE Adverse Event Report: ZIMMER BIOMET, INC. xsblyq bnsyecs bgyman epvdf qcfg