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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INC AMPLATZ EXTRA STIFF PTFE FIXED CORE WIRE GUIDE; OCY ENDOSCOPIC GUIDEWIRE, GASTROENTEROLOGY-UROLOGY

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COOK INC AMPLATZ EXTRA STIFF PTFE FIXED CORE WIRE GUIDE; OCY ENDOSCOPIC GUIDEWIRE, GASTROENTEROLOGY-UROLOGY Back to Search Results
Model Number N/A
Device Problem Material Fragmentation (1261)
Patient Problem Device Embedded In Tissue or Plaque (3165)
Event Date 09/13/2016
Event Type  malfunction  
Manufacturer Narrative
(b)(4).The event is currently under investigation.
 
Event Description
It was reported during a percutaneous nephrostolithotomy procedure for stone removal the coating was noted to be peeling off the product.Upon completion of the procedure, during check up, three small blue particles where seen inside the renal pelvis.The three small blue particles remain inside the renal pelvis.The patient did not require any additional procedures due to this occurrence.According to the initial reporter, the patient did not experience any adverse effects due to this occurrence.
 
Manufacturer Narrative
Investigation - evaluation: a review of the complaint history, device history record, specifications, quality control and visual inspection of the device was conducted during the investigation.The visual inspection of the device photo¿s reported that: a review of the supplied photo(s) reveals what appear to be areas where blue coating is sheared off.The complaint device was not returned therefore, no physical examinations could be performed; however, a document based investigation evaluation was performed.There is no evidence to suggest the product was not made to specifications.Investigation revealed that there were multiple nonconformances in the production process that were detected and scrapped in-house; however, this complaint is the first complaint from the field regarding this lot.A review of documentation revealed that in manufacturing the devices are 100% inspected for coating defects.Biocompatibility testing has been completed for the completed device.Risk assessment and escalation to review board determined that additional risk reduction was not required.A process change was previously initiated due to high occurrence rate of this failure mode and has now been implemented to improve the adherence of the ptfe coating to the wire guide.The complaint device was not produced via the improved process.Based on the information provided, the root cause of this complaint is determined to be manufacturing related and the appropriate personnel have been notified.We will continue to monitor for similar complaints.Per the quality engineering risk assessment no further action is required.
 
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Brand Name
AMPLATZ EXTRA STIFF PTFE FIXED CORE WIRE GUIDE
Type of Device
OCY ENDOSCOPIC GUIDEWIRE, GASTROENTEROLOGY-UROLOGY
Manufacturer (Section D)
COOK INC
750 daniels way
bloomington IN 47404
Manufacturer Contact
rita harden
750 daniels way
bloomington, IN 47404
8123392235
MDR Report Key6024198
MDR Text Key57213599
Report Number1820334-2016-01096
Device Sequence Number1
Product Code OCY
UDI-Device Identifier00827002535602
UDI-Public(01)00827002535602(17)190517(10)6923745
Combination Product (y/n)N
PMA/PMN Number
K082536
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor,foreign
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 09/13/2016
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 NumberN/A
Device Catalogue NumberAES-038145
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 09/13/2016
Initial Date FDA Received10/12/2016
Supplement Dates Manufacturer ReceivedNot provided
Supplement Dates FDA Received03/27/2017
Date Device Manufactured05/17/2016
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
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