STIMULAN RAPID CURE

Report

• Report Number: MW5180064
• Event Type: Injury
• Date Received: December 5, 2025
• Date of Event: November 14, 2025
• Report Date: December 2, 2025
• Manufacturer: BIOCOMPOSITES LTD.
• Product Code: MQV
• Adverse Event: Yes
• Report Source: Voluntary report
• Reporter Occupation: UNKNOWN
• Health Professional: *

Narratives

Description of Event or Problem · 0

EVENT DESCRIPTION: IT WAS REPORTED THAT BIPOLAR REMOVED BECAUSE OF INFECTION. NO OTHER INFORMATION AVAILABLE. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

Devices

Seq	Brand	Generic	Product Code	Manufacturer	Model	Lot	UDI-DI
130933	STIMULAN RAPID CURE	FILLER, BONE VOID, CALCIUM COMPOUND	MQV	BIOCOMPOSITES LTD.	620-010	SR240611

Patients

Seq	Age	Sex	Outcome	Treatment
1	NA	Unknown

Terms

Patient problem · 1

• Unspecified Infection

Product problems · 1

• Adverse Event Without Identified Device or Use Problem

Type of report · 1

• Initial submission