• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: OLYMPUS WINTER & IBE GMBH JAWS INSERT "HICURA", 5 X 330, METZENBAUM, MONOPOLAR; SCISSORS

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

OLYMPUS WINTER & IBE GMBH JAWS INSERT "HICURA", 5 X 330, METZENBAUM, MONOPOLAR; SCISSORS Back to Search Results
Model Number WA69370M
Medical Device Problem Code Connection Problem (2900)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event Malfunction
Event or Problem Description
The customer reported that his olympus hicura scissors were experiencing a connection issue.According to the initial reporter, shaft detaches from the handle and then the shaft inlay.As this occurs once the branchers are spread, the device cannot be removed from the trocar.Reportedly, the surgeon used a pair of pliers to close the branches of the hicura device, and then removed the inlay and pipe shaft.The customer did go on to note that this event has occurred ¿repeatedly¿.Please see report with patient identifier (b)(6) for related information.
 
Additional Manufacturer Narrative
The device has not been returned for evaluation.If additional information becomes available prior to the conclusion of the investigation, a supplemental report will be filed.
 
Additional Manufacturer Narrative
This report is being supplemented to provide additional information based on the legal manufacturer's final investigation.The device was returned to olympus for inspection, and the customer¿s complaint was confirmed.A review of the device history record found no deviations that could have caused or contributed to the reported issue.Based on the results of the investigation, the root cause of the reported event was determined to be the hicura scissors has a week point regarding the retaining function of the connection between jaw insert and handle regarding transmission of the cutting force.It is also assumed that over time the closing force drifted out of specification.Furthermore, it is also likely the high flexibility of the proximal end of the jaw insert, which is required to ensure an easy assembling of the instrument and to prevent damage of the proximal end, is also increasing the likelihood of the occurred phenomenon.A design change has been initiated to prevent further occurrences.Olympus will continue to monitor field performance for this device.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
JAWS INSERT "HICURA", 5 X 330, METZENBAUM, MONOPOLAR
Common Device Name
SCISSORS
Manufacturer (Section D)
OLYMPUS WINTER & IBE GMBH
kuehnstrasse 61
hamburg, hamburg 22045
GM  22045
Manufacturer (Section G)
OLYMPUS WINTER & IBE GMBH
kuehnstrasse 61
hamburg
Manufacturer Contact
todd brill
800 west park drive
westborough, MA 01581
5082077661
MDR Report Key17632130
Report Number9610773-2023-02365
Device Sequence Number20456013
Product Code GEI
UDI-Device Identifier04042761079761
UDI-Public04042761079761
Combination Product (Y/N)N
Initial Reporter CountryGM
PMA/510(K) Number
K140624
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)Unknown
Reporter Type Manufacturer
Report Source Other,Foreign,User Facility
Initial Reporter Occupation Other
Type of Report Initial,Followup
Report Date (Section B) 11/01/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberWA69370M
Device Lot NumberUNKNOWN
Was Device Available for Evaluation? Device Returned to Manufacturer
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/10/2023
Supplement Date Received by Manufacturer10/27/2023
Initial Report FDA Received Date08/28/2023
Supplement Report FDA Received Date11/01/2023
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured03/08/2022
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
-
-