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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BARD ACCESS SYSTEMS SM TI P.C. PORT W/INT.; IMPLANTABLE PORT
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BARD ACCESS SYSTEMS SM TI P.C. PORT W/INT.; IMPLANTABLE PORT Back to Search Results
Model Number 0602190
Medical Device Problem Code Migration or Expulsion of Device (1395)
Health Effect - Clinical Code No Consequences Or Impact To Patient (2199)
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
As the lot number for the device was not provided, a lot history review could not be performed.The sample was not returned to the manufacturer for inspection/evaluation.Therefore, the investigation is inconclusive for the reported migration.Based on the available information, the definitive root cause for this event is unknown.The device is labeled for single use.
 
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicates that model 0602190 implantable port allegedly experienced migration.The information was received from a single source.This malfunction involved one patient with no patient consequences.A (b)(6) patient weighs (b)(6).
 
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Brand Name
SM TI P.C. PORT W/INT.
Common Device Name
IMPLANTABLE PORT
Manufacturer (Section D)
BARD ACCESS SYSTEMS
605 n. 5600 w.
salt lake city UT 84116
MDR Report Key10737913
Report Number3006260740-2020-03477
Device Sequence Number11041441
Product Code LJT
UDI-Device Identifier00801741025549
UDI-Public(01)00801741025549
Combination Product (Y/N)N
Initial Reporter StateAZ
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 10/26/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device No Information
Device Model Number0602190
Device Catalogue Number0602190
Device Lot NumberUNKNOWN
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/30/2020
Initial Report FDA Received Date10/26/2020
Patient Sequence Number1
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