FDA Adverse Event Malfunction Summary report: N

ECLIPSE HOME PUMP

MDR report key: 55457 · Received December 13, 1996

Report

Report Number
MW1010399
Event Type
Malfunction
Date Received
December 13, 1996
Report Date
October 21, 1996
Manufacturer
BLOCK MEDICAL, INC.
Product Code
MEB
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

PT TRIED TO INFUSE A DOSE BUT PUMP WOULD NOT FUNCTION. PT USED ANOTHER HOME PUMP TO INFUSE. PHARMACY REPLACED DOSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ECLIPSE HOME PUMP ELASTOMERIC PUMP MEB BLOCK MEDICAL, INC. E101000-C UNK

Patients

Seq Age Sex Outcome Treatment
1 *