Per rep (b)(4) the customer stated that the patient came back in with indurated skin lesions.They wonder if the paclitaxel might be responsible for this.Did any unintended section of the device remain inside the patient¿s body? -no.If yes, please describe.Was the patient hospitalized or was there prolonged hospitalization due to this occurrence? -no.Did the patient require any additional procedures due to this occurrence? -no.If yes, please describe.Did the product cause or contribute to the need for additional procedures? -no.If yes, please specify additional procedures and provide details.Has the complainant reported any adverse effects on the patient due to this occurrence? -possibly.Has the complainant reported that the product caused or contributed to the adverse effects? -possibly.Please specify adverse effects and provide details.-indurated skin lesions.Prefix ziv6-ptx/zisv6-ptx: are images (e.G.Angiography, us etc.) of the device and/or procedure available? n/a, yes, no -no.Was the device flushed before the procedure, as per ifu? n/a, yes, no -yes.Were there any issues with flushing of the device? n/a, yes, no -no.Details of the access sheath used (name, fr size,length)? -g44154, lot 14813607.Details of the wire guide used (name, diameter, hyrdophyllic)? -.035, not cook, not hydrophilic.What approach was used to access the target site? contralateral, ipsilateral, antegrade, retrograde, other -contralateral.Please specify for other: if contralateral, was the bifurcation angle steep? n/a, yes, no -no.What was the target location for the stent? -left sfa.What artery was the stent placed in? proximal sfa, mid sfa, distal sfa, at the ostium of the profunda, p1 (proximal popliteal), other -entire sfa.Please specify for other: was the wire guide removed from the patient prior to advancing the delivery system? n/a, yes, no -no.If removed, was the wire guide wiped prior to advancement of the delivery system? n/a, yes, no -n/a.Did the stent delivery system cross the target location? n/a, yes, no -yes.Was pre-dilation performed ahead of placement of the stent? n/a, yes, no -yes.Was the patient¿s anatomy difficult or altered? previous bypass, tortuous, calcified, altered, other -no.If other, please specify: was resistance encountered when advancing the wire guide? n/a, yes, no -no.Was resistance encountered when advancing the delivery system to the target location? n/a, yes, no -no.Was resistance encountered when deploying the stent? n/a, yes, no -no.How did the physician deal with any resistance encountered? -no resistance.Was the stent fully deployed in the patient before removing the delivery system? n/a, yes, no -yes.After deployment did the stent show signs of any of the following: compression, fracture, deformation, constraint, elongation, other -no.If other, please specify: was post-dilation performed after the placement of the stent? n/a, yes, no -yes.Did any portion of the device break off? n/a, yes, no -no.If yes, please state what part: when did the device break? n/a, prep, advancement, deployment, withdrawal, after removal -n/a.Thumbwheel only ¿ was the distal end of the stability sheath inside the access sheath? n/a, yes, no -unkr.Thumbwheel only ¿ was the retraction sheet being held during deployment.N/a, yes, no -no.Did the thumbwheel spin freely or rotate without stent release or without retracting the stent retraction sheath? n/a, yes, no -it rotated freely and the stents deployed.If yes, was the stent partially deployed? n/a, yes, no -n/a.If yes, was the partially deployed stent removed with the delivery system or was it deployed in the patient? n/a, removed, deployed.If removed, did any part of the stent fracture during removal of the delivery system? n/a, yes, no -n/a.Was the delivery system kinked or twisted during advancement or deployment? n/a, yes, no -no.Please advise if and when any damage was observed on the; -n/a.Wireguide n/a, yes, no -n/a.Prior to use, during use, post procedure.Delivery system n/a, yes, no -no.Prior to use, during use, post procedur.E if yes, please specify (e.G.Kinked or twisted): what intervention (if any) was required? -none.Was the secondary intervention performed during the same procedure as the device failure or was it scheduled for another day? n/a, same procedure, another day -none were any other defects (other than the complaint issue) observed on the delivery system prior to return (e.G.Kink)? n/a, yes, no -no.Please specify if yes.
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