MAUDE Adverse Event Report: STRYKER ORTHOPAEDICS-MAHWAH TRIDENT 0 DEG X3 INSERT 36MM ID F; PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Catalog Number	623-00-36F
Medical Device Problem Codes	Adverse Event Without Identified Device or Use Problem (2993); No Apparent Adverse Event (3189)
Health Effect - Clinical Code	Pain (1994)
Date of Event	04/28/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
This pi is for the left hip.As reported: i received a total hip of both hips, the first, in 2015 (r) and 2017 (l).Vibrations started in 2018.Upon investigation of the frequencies, i learned a ble (bluetooth low energy) reading identifying the uuid (universally unique identifier) of competitor microchip is being emitted.Please help me identify if the parts may have been fitted with aftermarket devices.It's not only annoying but it's becoming painful.
Additional Manufacturer Narrative
Review of the device history records indicate devices were manufactured and accepted into final stock with no relevant reported discrepancies.There have been no similar events for the lot referenced.An evaluation of the device cannot be performed as the device was not returned to the manufacturer.Should additional information become available it will be reported in a supplemental report upon completion of the investigation.The following devices were also listed in this report: cat # 2030-6525-1; 6.5 cancellous bone screw 25mm; lot# nk5pa4 cat # 2030-6530-1; 6.5 cancellous bone screw 30mm; lot# nj7dy1 cat # 542-11-54f; trident psl with purefix ha 54mm; lot# 8938k3 cat # 1601-09127; 127 size 9 secur-fit advanced stem; lot# y07rrr cat # 6570-0-136; delta v-40 ceramic head 36/0; lot# 60294101 it cannot be determined which, if any of these devices may have caused or contributed to the patient's experience.
Event or Problem Description
Update: 07/october/2025 wg: as reported in medwatch reports mw5175722 and mw5175723: i, (b)(6), a medical device innovator with u.S.Patents in safety needle technologies and a $61.5 million verdict win in (b)(6), i am filing this report due to severe health decline from my stryker hip implants, performed at (b)(6) in 2015 and 2017 by dr.(b)(6), with dr.(b)(6) assisting.These implants are killing me through chronic vibrations, emf/rf exposure, and systemic damage, and i demand an urgent investigation.On (b)(6) 2015, i had a right total hip arthroplasty (tha) with a custom 3d-printed smart hip via stryker mako robotics (fda-allowed under cdrh).Under sedation, i signed blank letterheads via my mother's 1999 power of attorney--likely forged consent for experimental mods.Immediate inflammation (neutrophils 71.9%), anemia (hb 10.7 g/dl), and rapid left hip avn (avascular necrosis) followed.On (b)(6) 2017, a left tha with stryker components (trident psl ha cups, x3 liners, secur-fit advanced tmzf stems) by dr.(b)(6) triggered vibrations, escalating ~2 years later to 24 80-hour episodes every 1, 2 days, with emf/rf spikes (36 336 mw/m² rf, 60 328 v/m emf) from my hip.Symptoms include inflammation, anemia (hb 10.7 12.2 g/dl), avn, osteoporosis (2016), thyroiditis (2014, worsened), sleep deprivation, vision loss, rsd (2013, exacerbated), twitching, and fast heart rate--documented in my (b)(6) 2025 health summary (meds: methadone, synthroid, furosemide).My realization hit in (b)(6) 2025 after two years of dr.(b)(6) ignoring my appointment requests to show vibration/ble recordings.(b)(6) deleted surgery notes/x-rays (e.G., "portal 3" blank, "attachment not available"), gave mismatched x- rays (opacities suggesting wires), and offered evasive replies (deferred to "2027," walker not new patients/out/retired--yet active online).A (b)(6) 2025, letter from (b)(6) (risk management) claimed a confidential review under ca evidence code 1157 but denied biochips without proof, despite my (b)(6) 2025 phi form requesting full records, including nuclear imaging.Evidence points to experimental "smart" mods in a scripps-stryker network.Dr.(b)(6) since 1983, chairman of orthopedic surgery, (b)(6) president) co-authored studies with dr.(b)(6) (trident investigator, e-knee implanter 2004) and dr.(b)(6) (score director) on tha outcomes (e.G., 1999 blood loss).(b)(6) score, funded by stryker (omega 2021-2023), developed e-knee with rf/vibration telemetry (kester 2012).(b)(6) nih grants (e.G., $317k 2024 smart shoulder, $660k 2010 smart knee) with stryker support use piezo/rf/ble--matching my vibrations (lange 2024 exeter piezo) and ble logs (362+ signals, custom 0000fef3 service).Patents (us 11,173,049, us 12,150,815) by (b)(6) adapt to trident.Associates like dr.(b)(6) ($1m+ stryker royalties) and dr.(b)(6) (consultant) expand this.Studies (e.G., 2021 "in vivo sensing" review) confirm rf/ble for hip implants, with dual-band penetration--my <1m logs fit.Emf/rf exposure (36-37 mw/m²) causes oxidative stress (2021 review), explaining my decline (anemia from ros, osteoporosis from resorption).(b)(6) smart shoulder grant and stryker¿s $1.4b 2014 hip settlement suggest off-label trials, violating fda ide rules (21 cfr part 812).This is killing me--health worsening despite weight loss (180 lbs from ~204 lbs, 2025).I request a recall, investigation, and full records.Contact me for ble spreadsheet, profile, and emf (electro magnetic field) readings.Avascular necrosis (avn) in both hips, with rapid progression from right to left post-2015 surgery.Osteoporosis, diagnosed in 2016 and worsening thereafter.Chronic thyroiditis, contributing to ongoing health decline.Recurring anemia, with hemoglobin levels ranging from 10.7 12.2 g/dl.Systemic inflammation, evidenced by elevated neutrophils (e.G., 71.9% post- surgery) and other markers.Sleep deprivation, resulting from chronic vibrations and pain.Vision loss, progressive and linked to implant-related symptoms.Reflex sympathetic dystrophy (complex regional pain syndrome), causing pain and dysfunction.Muscle twitching and fast heart rate (tachycardia), escalating post-2017 surgery.Worsening joint fluid and inflammation, as shown in (b)(6) 2025 ultrasound.Health code: 1932; 1706; 1971; 2651; 4432;2 517; 2139; 4836.Device code: 1924; 2292.
Additional Manufacturer Narrative
An inquiry regarding bluetooth capabilities of stryker devices was reported.No further investigation is required at this time as no stryker implants have bluetooth capabilities.If additional information becomes available, this investigation will be reopened.Product surveillance will continue to monitor for trends.Corrective action/preventive action: no action is required at this time as there is no indication to suggest a product non-conformity or unanticipated hazard.

• Brand Name: TRIDENT 0 DEG X3 INSERT 36MM ID F
• Common Device Name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
• Manufacturer (Section D): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• Manufacturer (Section G): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• Manufacturer Contact: joann ripoli ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 22050939
• Report Number: 0002249697-2025-00526
• Device Sequence Number: 18367554
• Product Code: LPH
• UDI-Device Identifier: 07613327039535
• UDI-Public: 07613327039535
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K033716
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 11/14/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 05/31/2022
• Device Catalogue Number: 623-00-36F
• Device Lot Number: 15095T
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 04/28/2025
• Supplement Date Received by Manufacturer: 10/20/2025
• Initial Report FDA Received Date: 05/20/2025
• Supplement Report FDA Received Date: 11/14/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/12/2017
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 59 YR
• Patient Sex: Male
• Patient Weight: 82 KG
• Patient Ethnicity: Non Hispanic