MAUDE Adverse Event Report: C.R. BARD, INC. (GFO) LUTONIX 035 DRUG COATED BALLOON PTA CATHETER

Model Number 9004

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Intimal Dissection (1333)

Event Type  Injury  

Manufacturer Narrative

Analysis: the samples were not returned from the user facility; therefore, device evaluations are unable to be performed.The lot history review could not be conducted because the lot number, although requested, was not available from the user facility.The dhr review also was not conducted because the facility did not provide the lot number.Conclusion: the actual samples were not returned for evaluation.The dhr review was not conducted because the facility did not provide the lot number.Based on the instructions for use (ifu), the occurrence of dissection is an inherent risk of any pta procedure.If additional information becomes known to the manufacturer, a supplemental report will be provided with all relevant information.

Event Description

It was reported through a literature article that during the index procedure, three lutonix percutaneous transluminal drug coated balloon (dcb) dilatation catheters were used to treat the target lesion in the superficial femoral artery (sfa) and popliteal artery.After systemic anticoagulation with heparin, the lesion was crossed intraluminally with a v-18 control wire guidewire (boston scientific, marlborough, mass) and a spider embolic protection device (medtronic, marlborough minn) was deployed in the distal popliteal artery.A distal filter was used because multiple filling defects seen on duplex ultrasound (dus) presented a potential embolic source.Sfa and popliteal artery were pre-dilated with an armada 0.018-inch 3mm x 200mm balloon and an armada 0.018-inch 5mm x 200mm balloon (abbott vascular, abbott park iii).Then, the lesions were treated with three lutonix dcb's (c.R.Bard, murray hill, nj).The lengths of the balloons were 5mm x 150mm, 5mm x 150mm, and 8mm x 50mm.Digital subtraction angiography demonstrated a new flow-limiting dissection in distal sfa after angioplasty.A 6mm x 80mm eluvia drug-eluting stent (boston scientific) was placed to cover the dissection with primary complete expansion.There was an excellent final angiographic result with no residual stenosis in the sfa.The lutonix dcb's were discarded by the user facility.No further adverse patient outcomes were reported.This is one of three products involved with the reported event and the associated manufacturer¿s report numbers are 3006513822-2019-00031 and 3006513822-2019-00032.

• Brand Name: LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
• Type of Device: DRUG COATED BALLOON PTA CATHETER
• Manufacturer (Section D): C.R. BARD, INC. (GFO); 289 bay road; queensbury NY 12804
• Manufacturer (Section G): C.R. BARD, INC. (GFO); 289 bay road; queensbury NY 12804
• Manufacturer Contact: mike gaffney ; 9409 science center dr; new hope, MN 55428 ; 7634458639
• MDR Report Key: 8388051
• MDR Text Key: 137850430
• Report Number: 3006513822-2019-00033
• Device Sequence Number: 1
• Product Code: ONU
• UDI-Device Identifier: 00801741166310
• UDI-Public: (01)00801741166310
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: P130024
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor,foreign,literatur
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 03/04/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: 9004
• Device Catalogue Number: 9090475800060
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Event Location: Hospital
• Initial Date Manufacturer Received: 02/06/2019
• Initial Date FDA Received: 03/04/2019
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 76 YR