DUROLANE

Report

• Report Number: MW5181198
• Event Type: Other
• Date Received: December 26, 2025
• Date of Event: December 18, 2025
• Report Date: December 18, 2025
• Manufacturer: BIOVENTUS LLC
• Product Code: MOZ
• Report Source: Voluntary report
• Reporter Location: FL, US
• Reporter Occupation: NURSE
• Health Professional: Yes

Narratives

Description of Event or Problem · 0

PATIENT REPORTS PAIN TO BOTH KNEES (PAIN LEVEL 6/10 TO 7/10) WHEN SHE WALKS AFTER SHE RECEIVED THE DUROLANE INJECTION RIGHT KNEE AND CORTISONE INJECTION LEFT KNEE YESTERDAY. UNILATERAL PRIMARY OSTEOARTHRITIS.

Devices

Seq	Brand	Generic	Product Code	Manufacturer	Model	Lot	UDI-DI
2319722	DUROLANE	ACID, HYALURONIC, INTRAARTICULAR	MOZ	BIOVENTUS LLC

Patients

Seq	Age	Sex	Outcome	Treatment
1	67 YR	Female		ATORVASTATIN.| ESTRADIOL TRANSDERMAL GEL.| PANTOPRAZOLE.| SERTRALINE.

Terms

Patient problem · 1

• Pain

Product problems · 1

• Adverse Event Without Identified Device or Use Problem

Type of report · 1

• Initial submission