FDA Adverse Event Injury Summary report: N

MEDVANCE SILICONE FOAM, BOARDERED SILICONE FOAM DRESSING

MDR report key: 17070948 · Received June 5, 2023

Report

Report Number
MW5118177
Event Type
Injury
Date Received
June 5, 2023
Date of Event
April 23, 2023
Report Date
June 1, 2023
Manufacturer
MED WAY INC.
Product Code
NAD
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
MA, US
Reporter Occupation
UNKNOWN
Health Professional
*

Narratives

Description of Event or Problem · 0

WERE HURT OR HAD A BAD SIDE EFFECT (INCLUDING NEW OR WORSENING SYMPTOMS. HOSPITALIZATION), - ADMITTED OR STAYED LONGER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1093511 MEDVANCE SILICONE FOAM, BOARDERED SILICONE FOAM DRESSING DRESSING, WOUND, OCCLUSIVE NAD MED WAY INC. 20211125

Patients

Seq Age Sex Outcome Treatment
1 95 YR Female Hospitalization| S| L