FDA Adverse Event Injury Summary report: N

ZEVEX INFINITY PUMP

MDR report key: 1917936 · Received December 3, 2010

Report

Report Number
MW5018496
Event Type
Injury
Date Received
December 3, 2010
Date of Event
July 19, 2010
Report Date
December 3, 2010
Manufacturer
MOOG
Product Code
LZH
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
GA, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

ZEVEX ENTERAL PUMP ALARMING 'NO FOOD'. (B)(6), RN AT BEDSIDE. TROUBLESHOOTING WITH TRIAGE NURSE PER MANUAL. (B)(6) RN STATES HE HAS THE NEWEST MANUAL AT BEDSIDE AND HAS BEEN TROUBLESHOOTING PUMP FOR 60 MIN PER MANUAL FOR 'NO FOOD' ALARM, WITH NO RESOLUTION. INSTRUCTED CALLER TO CONTINUE BOLUS FEEDINGS AT THE PRESCRIBED RATE: 125 ML PER HOUR, OR 60 ML EVERY 30 MIN. CALLER REQ NEW PUMP FOR TOMORROW (B)(6) 2010. DIAGNOSIS OR REASON FOR USE: SPINAL MUSCULAR ATROPHY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ZEVEX INFINITY PUMP ENTERAL PUMP LZH MOOG 507164081

Patients

Seq Age Sex Outcome Treatment
1 12 YR Disability