FDA Adverse Event Injury Summary report: N

AQUA-EEZ

MDR report key: 446134 · Received February 18, 2003

Report

Report Number
446134
Event Type
Injury
Date Received
February 18, 2003
Date of Event
January 25, 2003
Report Date
February 4, 2003
Manufacturer
AQUA - EEZ, INC
Product Code
ILJ
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
NH, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

DELIVERY INITIATED IN BIRTHING TUB. PT MOVED TO BED TO COMPLETE DELIVERY. TUB FAILED TO DRAIN ACCORDING TO GUIDELINES. APGAR 5,8. BABY DELIVERED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AQUA-EEZ BIRTHING TUB ILJ AQUA - EEZ, INC 3020 *

Patients

Seq Age Sex Outcome Treatment
1 0 DAY Hospitalization