FDA Adverse Event Injury Summary report: N

RESQPUMP

MDR report key: 5496414 · Received March 11, 2016

Report

Report Number
3000143502-2016-00002
Event Type
Injury
Date Received
March 11, 2016
Date of Event
December 10, 2015
Report Date
March 11, 2016
Manufacturer
ADVANCED CIRCULATORY
Product Code
PIZ
PMA / PMN Number
P110024
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

A (B)(6) FEMALE, CARDIAC ARREST, POSSIBLE PNEUMOTHORAX.

Description of Event or Problem · 1

A (B)(6) FEMALE, CARDIAC ARREST, POSSIBLE PNEUMOTHORAX.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
152539 RESQPUMP RESQPUMP PIZ ADVANCED CIRCULATORY 12-0823-000

Patients

Seq Age Sex Outcome Treatment
1 69 YR Other