ULTRACLAMP TUBING CLAMP 5C4957

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-09 for ULTRACLAMP TUBING CLAMP 5C4957 manufactured by Baxter Healthcare Corporation.

Event Text Entries

[174474209] The event occurred on an unspecified date in (b)(6) 2019. The device was discarded and the lot number is unknown; therefore, a device analysis could not be completed. Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[174474210] It was reported that the two (2) ultra clamps leaked from an unspecified location. This occurred during filling of peritoneal dialysis therapy. It was further reported that "the red clamp did not fully close off the tube and fluid passed into the drain bag. " there was no patient injury or medical intervention associated with this event. No additional information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1416980-2019-07484
MDR Report Key9570616
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-09
Date of Report2020-01-09
Date Mfgr Received2019-12-18
Date Added to Maude2020-01-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - CLEVELAND
Manufacturer Street911 HIGHWAY 61 NORTH PO BOX 1058
Manufacturer CityCLEVELAND MS 38732
Manufacturer CountryUS
Manufacturer Postal Code38732
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameULTRACLAMP TUBING CLAMP
Generic NameCLAMP, LINE
Product CodeFKK
Date Received2020-01-09
Model NumberNA
Catalog Number5C4957
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE CORPORATION
Manufacturer AddressDEERFIELD IL


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-09

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