FDA Adverse Event Injury Summary report: N

DEPUY KNEE IMPLANT

MDR report key: 7302383 · Received February 27, 2018

Report

Report Number
MW5075561
Event Type
Injury
Date Received
February 27, 2018
Manufacturer
DEPUY
Product Code
JWH
Report Source
Voluntary report
Reporter Location
MS, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

HAD KNEE REPLACEMENT DEPUY IN 2016 KNEE SHARP WARM AND I HAVEN'T BEEN ABLE TO THINK CLEARLY LIKE SOME TYPE OF TOXIN. THEN THEY GAVE ME (B)(6), TOLD ME IT WAS MY (B)(6) NEVER TOOK BUN. QUEST DIAGNOSTICS, NONE COVERED BY FEDERAL DRUG AND ADMIN. CAN'T GET ANYONE TO RUN LAST SET OF LAB WORK UPS ISSUED BY PRIMARY CARE. THEY SAID THE CRAZY MIND EFFECT WAS FROM MY (B)(6), SO THEY GAVE ME (B)(6) BUT IT STILL HAPPENS LIKE TOXIN COMING FROM MY KNEE. I HAD A KNEE REPLACEMENT; WHAT DID THEY DO TO ME. PLEASE HELP. HAD A KNEE REPLACEMENT. DEPUY SEEMS LIKE IT'S EMITTING SOME TYPE OF RADIATION OR TOXIN IN MY BODY. HAS ME MENTALLY CONFUSED. PAIN, SWELLING, CRACKING AND POPPING. AFTER GENESIGHT TESTING THROUGH DR (B)(6) OFFICE, I HAD A KNEE REPLACEMENT. IT'S NEVER BEEN THE SAME. IN 2016, I EXPERIENCED WHAT SEEMED LIKE "GASING", I COULD SEE WAVES IN THE AIR AND MY MENTAL STATE WAS CRAZY. (B)(6) TOOK ME TO GET LAB WORK DONE AND THEY DECIDED THAT IT WAS MY (B)(6). THEY GAVE ME (B)(6). I HAVE STILL HAD COMPLICATION. I HAD TO TELL DR (B)(6), HE IGNORED IT. FINALLY I GOT THEM TO DO LAB WORK ORDER, THE ONE BELOW.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
141835 DEPUY KNEE IMPLANT DEPUY KNEE IMPLANT JWH DEPUY

Patients

Seq Age Sex Outcome Treatment
1 53 YR Hospitalization| S