MalfunctionMOZ
DUROLANE
Received Jul 17, 2025 · Event occurred Jun 24, 2025
Report 22529904 · MDR key 22529904
Device
Generic name
Acid, Hyaluronic, Intraarticular
Manufacturer
Bioventus LlcModel number
1082020Catalog number
1082020
Lot number
23172
Product problems
- Use of Device Problem
Patient
58 YR · Male
- Pain
- Ambulation or Postural Difficulties
- Swelling/ Edema
- Pain
- Ambulation or Postural Difficulties
- Swelling/ Edema
Narrative
Description of Event or Problem
ON [DATE REDACTED] PT RECEIVED A DUROLANE INJECTION TO THE L [LEFT] KNEE IN THE [REDACTED] ORTHOPEDIC OFFICE. NO IMMEDIATE COMPLICATIONS WERE NOTED POST-INJECTION. ON [DATE REDACTED] -- 2 DAYS AFTER INJECTION, THE PT CALLED THE OFFICE REPORTING HE WAS EXPERIENCING SWELLING, INABILITY TO WEIGHT BEAR, AND EXTREME PAIN. PT REPORTED WAS RESTING THE KNEE, USING ICE, ELEVATING THE EXTREMITY, AND TAKING/EXCEEDING THE NORMAL AMOUNT OF ADVIL WITHOUT RELIEF.