BONE GRAFT
Received Jul 29, 2025 · Event occurred Dec 6, 2021
Report MW5173493 · MDR key 22646537
Device
Generic name
Filler, Bone Void, Calcium Compound
Manufacturer
Bioventus LlcProduct problems
- Adverse Event Without Identified Device or Use Problem
Patient
43 YR · Female
- Pain
- Stenosis
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
- Pain
- Stenosis
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
Narrative
Description of Event or Problem
REPORTER CALLED TO SUBMIT A REPORT ABOUT HER IMPLANTED DEVICES. SHE SAID ONE DAY SHE WAS WALKING, AND SHE EXPERIENCED SHOOTING PAIN, AND SHE WENT TO EMERGENCY ROOM. SHE SAID SHE WAS REFERRED TO (B)(6). SHE SAID THE ORTHOPEDIC DIAGNOSED HER WITH DEGENERATIVE DISC DISEASED, SPINAL STENOSIS, HERNIATED DISC. THE DOCTOR PRESCRIBED PAIN MEDICATION FOR HER PAIN. THE DOCTOR TOLD HER THAT SHE NEEDS A PROCEDURE CALLED POSTERIOR SPINAL FUSION WITH DECOMPRESSION. SHE SAID THE PAIN MEDICATION DID NOT ALLEVIATE HER PAIN. SHE WAS HAVING AN ONGOING PAIN. SHE SAID THE DOCTOR TOLD HER HE NO LONGER CARES FOR HER BECAUSE OF HER INSURANCE. PATIENT CODES: 1994, 2263, 4581. DEVICE CODE: 2993. REFERENCE REPORTS: #MW5173489, #MW5173490, #MW5173491, #MW5173492.