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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BARD ACCESS SYSTEMS POWERPICC SOLO HF CATHETER WITH SHERLOCK 3CG TIP POSITIONING SYSTEM (TPS) STYLET; CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS

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BARD ACCESS SYSTEMS POWERPICC SOLO HF CATHETER WITH SHERLOCK 3CG TIP POSITIONING SYSTEM (TPS) STYLET; CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS Back to Search Results
Model Number 1395108QD
Device Problem Malposition of Device (2616)
Patient Problems Respiratory Distress (2045); Vomiting (2144)
Event Date 10/13/2018
Event Type  malfunction  
Manufacturer Narrative
The following were reviewed as part of this investigation: patient severity, frequency analysis, applicable previous investigation(s), sample (if available), applicable fmea documents, labeling, and applicable manufacture records.Based on a review of this information, the following was concluded: the complaint of catheter malposition was inconclusive because no sample was returned for evaluation.Based on the description of the reported event, possible contributing factors include anatomical features and changes in thoracic pressure; however, the lack of a returned sample prevented both confirmation of the reported event and identification of a root cause(s).Consequently, this complaint is inconclusive at this time.A lot history review (lhr) of recu0224 showed no other similar product complaint(s) from this lot number.
 
Event Description
Per (b)(6): nurse states on (b)(6) 2018, icu patient powerpicc solo placed using with sherlock 3cg tip locating system.Placement was confirmed to be in the lower 1/3 svc at right atrium.Nurse states the powerpicc solo was placed in the left brachial vein.The nurse states patient has pancreatitis, sepsis and pleural effusion.She states the next morning on (b)(6) 2018, an x-ray was performed and it was determined that the powerpicc solo had malposition up the chest into the right sibclavian vein.She is asking how this might happen.(b)(6) informed caller that increase in thoracic pressure by coughing or vomiting can increase risk for malposition of the tip of a picc.Informed that some facilities nurses will fast flush the powerpicc and see if it can be dropped and a repeat x-ray will be needed.Informed radiology could be contacted to look at the tip location and guide the powerpicc down to needed tip placement.(b)(6) 2018, additional details: the line malpositioned one more time on (b)(6) 2018, the line was pulled out to the point of a midline placement.There has not been any other issues with the catheter was a midline.
 
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Brand Name
POWERPICC SOLO HF CATHETER WITH SHERLOCK 3CG TIP POSITIONING SYSTEM (TPS) STYLET
Type of Device
CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS
Manufacturer (Section D)
BARD ACCESS SYSTEMS
605 n. 5600 w.
salt lake city UT 84116
Manufacturer (Section G)
BARD REYNOSA S.A. DE C.V. -9617592
blvd. montebello #1
parque industrial colonial
reynosa, tamaulipas
MX  
Manufacturer Contact
heather murphy
605 n. 5600 w.
salt lake city, UT 84116
8015225738
MDR Report Key8044149
MDR Text Key126595464
Report Number3006260740-2018-03160
Device Sequence Number1
Product Code LJS
UDI-Device Identifier00801741034725
UDI-Public(01)00801741034725
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K091324
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Reporter Occupation Nurse
Type of Report Initial
Report Date 11/06/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/06/2018
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number1395108QD
Device Catalogue Number1395108QD
Device Lot NumberRECU0224
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Event Location Hospital
Date Manufacturer Received10/15/2018
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured07/01/2018
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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