FDA Adverse Event Malfunction Summary report: N

MEDICAL ACTION LIGHT SHIELD, SEMI-RIGID, NON-STERILE

MDR report key: 6901947 · Received September 28, 2017

Report

Report Number
1836161-2017-00106
Event Type
Malfunction
Date Received
September 28, 2017
Date of Event
February 9, 2017
Report Date
September 28, 2017
Manufacturer
ASPEN SURGICAL PRODUCTS, CALEDONIA
Product Code
FTA
PMA / PMN Number
K020304
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE NOT AVAILABLE.

Description of Event or Problem · 1

COMPLAINT (B)(4) ON ITEM NB8000. LIGHT SHIELD CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
680614 MEDICAL ACTION LIGHT SHIELD, SEMI-RIGID, NON-STERILE LIGHT SHIELD FTA ASPEN SURGICAL PRODUCTS, CALEDONIA NB8000 114900

Patients

Seq Age Sex Outcome Treatment
1