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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BARD ACCESS SYSTEMS OTW, 14.5 FR, 23CM, ST, SPLIT TIP, STANDARD KIT; DIALYSIS CATHETER

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BARD ACCESS SYSTEMS OTW, 14.5 FR, 23CM, ST, SPLIT TIP, STANDARD KIT; DIALYSIS CATHETER Back to Search Results
Model Number 5903230
Medical Device Problem Code Defective Component (2292)
Health Effect - Clinical Code No Patient Involvement (2645)
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
As the lot number for the device was provided, a review of the device history records is currently being performed.The device has been returned to the manufacturer for evaluation.The investigation of the reported event is currently underway.
 
Event or Problem Description
It was reported that prior to hemodialysis catheter placement, the tunneler tip broke off and was rendered unusable.It was further reported that another device was used to perform the procedure.There was no reported patient contact.
 
Additional Manufacturer Narrative
Manufacturing review: the lot met all release criteria.Manufacturing records were reviewed (dhr, mrr¿s, scrap and mfg.Process changes) and there were not found evidence that the failure mode reported in this complaint is caused by the mfg.Process.Investigation summary: one equistream d/l catheter along with tunneler in two segments, peel-apart sheath and dilator, two additional dilators, an end cap, and a guidewire in hoop was returned for evaluation.Visual and microscopic evaluations were performed.The investigation is confirmed for damaged/defective tunneler, as the the proximal plastic end of the tunneler was received broken from the device.Microscopic evaluation revealed more detail on the break surface on the proximal end of the plastic.Cracking was observed on the break surface.The surface was observed to be mostly smooth in texture.No obvious tool damage was observed on the outer surface of the plastic.The definitive root cause for the reported damaged tunneler issue could not be determined based upon available information.It is unknown whether patient and/or procedural issues contributed to the event.However, vt-sca-19-4398 is currently opened to address the issue and identify appropriate actions.Labeling review: a review of product labeling documents (e.G.Procedural instructions, indications, warnings, precautions, cautions, possible complications, contraindications, nursing guide, and unit label) showed that the product labeling is adequate.
 
Event or Problem Description
It was reported that prior to hemodialysis catheter placement, the tunneler tip broke off and was rendered unusable.It was further reported that another device was used to perform the procedure.There was no reported patient contact.
 
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Brand Name
OTW, 14.5 FR, 23CM, ST, SPLIT TIP, STANDARD KIT
Common Device Name
DIALYSIS CATHETER
Manufacturer (Section D)
BARD ACCESS SYSTEMS
605 n. 5600 w.
salt lake city UT 84116
MDR Report Key8406192
Report Number3006260740-2019-00526
Device Sequence Number297964
Product Code MSD
UDI-Device Identifier00801741013706
UDI-Public(01)00801741013706
Combination Product (Y/N)N
Initial Reporter StatePA
Initial Reporter CountryUS
PMA/510(K) Number
K090101
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date (Section B) 04/23/2019
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 Health Professional
Device Model Number5903230
Device Catalogue Number5903230
Device Lot NumberRECX3053
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer02/27/2019
Initial Date Received by Manufacturer 02/13/2019
Supplement Date Received by Manufacturer04/05/2019
Initial Report FDA Received Date03/08/2019
Supplement Report FDA Received Date04/23/2019
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
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