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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RICHARD WOLF GMBH E-LINE; URETERORENOSCOPE 5° 6/7.5FR WL 430MM

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RICHARD WOLF GMBH E-LINE; URETERORENOSCOPE 5° 6/7.5FR WL 430MM Back to Search Results
Model Number 8702534
Device Problem Poor Quality Image (1408)
Patient Problem Insufficient Information (4580)
Event Date 08/05/2023
Event Type  Injury  
Manufacturer Narrative
The examination has revealed that moisture has penetrated into system at the sealing ring.The ureterorenoscope 5° 6/7.5fr wl 430mm, part id: 8702534, serial # (b)(6), was produced on (b)(6) 2022 in a lot of (b)(4) pieces.Until today, this is the only s/n (b)(6) from this lot which was claimed with this error pattern.The defect is considered as a sporadic failure.In the last three years, a total of 6 complaints were processed for this type, which were also classified as sporadic failures.At the same time, (b)(4) types were sold worldwide.Based on this data, we do not see any fundamental problem, the instrument corresponds to the current state of the art.The ifu ga-d 352 /usa/ 2012-11 v4.0 i eco: 2012-0540 contains several descriptions of visual and functional checks which serve to detect faults prior to use on patient in section 7 use and section 8 checks.In additional, the ifu states that there must always be an operable comparable device or a conventional system on hand.The subject issue of image failure is present in the risk management file a1 - reusable rigid optics with and without working channel, rev.05.The overall probability of occurrence for this issue remains at previously defined levels and overall risk of the device remains in the acceptable category.
 
Event Description
The user facility has informed richard wolf gmbh of an issue regarding a ureterorenoscope 5° 6/7.5fr wl 430mm, part id: 8702534, serial number # (b)(6).Surgery planned on august 5, 2023, resolution of patient case with ureteral lithiasis, ureteral lithotripsy surgery is planned using richard wolf ureterorenoscope 5° 6/7.5fr.According to the initial reporter, the procedure begins, perceiving poor image quality at the beginning of the procedure, with the presence of an external halo that reduces the field of vision, making maneuvers within the ureter difficult.An attempt is made to perform lithotripsy with a pneumatic lithotripter; due to vision difficulties, it is decided to suspend procedure and reschedule the case until a new work item is available, exposing the patient again to another anesthetic event and another hospitalization.There was a time delay about 90 minutes.
 
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Brand Name
E-LINE
Type of Device
URETERORENOSCOPE 5° 6/7.5FR WL 430MM
Manufacturer (Section D)
RICHARD WOLF GMBH
pforzheimer strasse 32
d-75438 knittlingen, germany
GM 
Manufacturer (Section G)
RICHARD WOLF GMBH
pforzheimer strasse 32
knittlingen, germany 75438
GM   75438
Manufacturer Contact
valentin felsing
pforzheimer strasse 32
knittlingen, germany 75438
GM   75438
MDR Report Key17920799
MDR Text Key325500215
Report Number9611102-2023-00058
Device Sequence Number1
Product Code FGB
UDI-Device Identifier04055207020036
UDI-Public04055207020036
Combination Product (y/n)N
Reporter Country CodeMX
PMA/PMN Number
K062720
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,User Facility
Reporter Occupation Other
Remedial Action Repair
Type of Report Initial
Report Date 10/12/2023
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 Number8702534
Device Catalogue Number8702.534
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer09/20/2023
Initial Date Manufacturer Received 10/05/2023
Initial Date FDA Received10/12/2023
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured05/23/2022
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Outcome(s) Other;
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