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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DAVIS & GECK CARIBE LTD ENDO CLIP II; CLIP, IMPLANTABLE

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DAVIS & GECK CARIBE LTD ENDO CLIP II; CLIP, IMPLANTABLE Back to Search Results
Model Number 176657
Device Problems Mechanical Problem (1384); Difficult to Open or Close (2921)
Patient Problem No Patient Involvement (2645)
Event Date 09/27/2019
Event Type  malfunction  
Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
 
Event Description
According to the reporter, prior to use on a laparoscopic cholecystectomy procedure, the jaws of the device did not close but still could fire.The device essentially shot out fully opened clips onto the table.A new clip applier was used to complete the procedure.There was no patient involvement.
 
Manufacturer Narrative
Evaluation summary: post market vigilance (pmv) led an evaluation of one device.The instrument was received partially applied with two remaining clips.During functional evaluation, it was observed that the jaws would not close upon actuation of the handle.The instrument body was removed from the shaft and disassembled for visualization of internal components.It was observed that the firing handle linkage was forced through the channel tube lugs, suggesting that the instrument had been fired through the safety interlock.The instrument shaft was reassembled into an instrument body from the pmv inventory and applied to appropriate test media.Clips advanced into the jaws, formed properly, and were held securely in place after full formation was achieved and the firing handle was released.When the cartridge was empty, the interlock engaged to prevent the jaws from approximating.Due to the noted damage, further functional testing of the instrument was not performed.Records from each manufacturing lot are thoroughly reviewed to ensure that products are released meeting all quality release specifications at the time of manufacture.Replication of the broken firing linkage condition may occur under the following conditions: 1) when the firing handle has not been allowed to fully return to the home position after forming a previous clip.2) a single continuous handle compression is one of two firing methods described in the information booklet which accompanies each product shipment, if the handle is compressed at an accelerated rate, clips do not have enough time to enter the jaws and the instrument will lock preventing the jaws from closing without a clip.The instructions for use (ifu) warns to confirm that the clip is positioned within the jaws and is free of other clips or obstructions before squeezing the handle top close the clip.However, rather than forceful compression of the firing handle under these circumstances, if the firing handle is fully released by relieving hand pressure, the interlock feature will disengage, the next clip will load, and the clip can be applied.Furthermore; if an attempt is made to forcibly fire the instrument while engaged in interlock after all the clips has been fired, the lugs are designed to break as noted.The root cause of the observed damage was due to the product not being used as intended which caused or contributed to the reported condition.No further actions have been deemed necessary at this time.Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
 
Event Description
According to the reporter, prior to use on a laparoscopic cholecystectomy procedure, the jaws of the device did not close but still could fire.The device essentially shot out fully opened clips onto the table.A new clip applier was used to complete the procedure.There was no patient involvement.
 
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Brand Name
ENDO CLIP II
Type of Device
CLIP, IMPLANTABLE
Manufacturer (Section D)
DAVIS & GECK CARIBE LTD
zona franca de san isidro
santo domingo 0101
DO  0101
MDR Report Key9197743
MDR Text Key162903940
Report Number9612501-2019-02003
Device Sequence Number1
Product Code FZP
UDI-Device Identifier10884521057869
UDI-Public10884521057869
Combination Product (y/n)N
PMA/PMN Number
K954435
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,user f
Type of Report Initial,Followup
Report Date 11/27/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/16/2019
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number176657
Device Catalogue Number176657
Device Lot NumberJ9G2687NY
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer10/01/2019
Date Manufacturer Received11/12/2019
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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