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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION SPECTRUM INFUSION PUMP
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BAXTER HEALTHCARE CORPORATION SPECTRUM INFUSION PUMP Back to Search Results
Model Number 35700
Device Problem Difficult to Open or Close (2921)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 01/01/2015
Event Type  malfunction  
Event Description
It was reported that a spectrum pump had a latch not closing.It was also reported there was no patient injury.
 
Manufacturer Narrative
Manufacturer ref no.: (b)(4).Baxter received and evaluated the device.The device was found out of specification with respect to the latch not closing, which was reproduced while attempting to load a set.Evaluation experienced a door not fully latched alarm while attempting to load a set.The symptom was confirmed through a review of the device event history log.The messages were found to be caused by loose lower link screws.The link screws were replaced.
 
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Brand Name
SPECTRUM INFUSION PUMP
Type of Device
INFUSION PUMP
Manufacturer (Section D)
BAXTER HEALTHCARE CORPORATION
medina NY
Manufacturer Contact
kelly morse, sr.mgr., quality
711 park ave.
medina, NY 14103-0756
8003563454
MDR Report Key4706919
MDR Text Key5651024
Report Number1314492-2015-03302
Device Sequence Number1
Product Code FRN
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K042121
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Biomedical Engineer
Remedial Action Repair
Type of Report Initial
Report Date 02/11/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/06/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number35700
Device Catalogue Number35700
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer01/28/2015
Is the Reporter a Health Professional? Yes
Date Manufacturer Received02/11/2015
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured09/26/2011
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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