MAUDE Adverse Event Report: STRYKER INSTRUMENTS-INAGI SONOPET STRAIGHT HANDPIECE, UNIVERSAL; INSTRUMENT, ULTRASONIC SURGICAL

Catalog Number	5450840000
Medical Device Problem Code	Overheating of Device (1437)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	01/01/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events: 3 events were reported for this quarter.  product return status: 3 devices were received.  event confirmation status : 3 device evaluations are still in progress.Additional information : 3 devices were not labeled for single-use.3 devices were not reprocessed and reused.
Event or Problem Description
This report summarizes 3 malfunction events in which the device reportedly overheated.1 event had no patient involvement; no patient impact.1 event had patient involvement; no patient impact.1 event had no known patient impact or consequences.
Event or Problem Description
This report summarizes 3 malfunction events in which the device reportedly overheated.1 event had no patient involvement; no patient impact.1 event had patient involvement; no patient impact.1 event had no known patient impact or consequences.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Supplemental rationale corrected data: h10 3 previously reported events are included in this follow-up record.Product return status 3 devices were received.Event confirmation status 3 reported events were not confirmed.Evaluation results 3 devices were found to be affected by customer exceeding duty cycle.

• Brand Name: SONOPET STRAIGHT HANDPIECE, UNIVERSAL
• Common Device Name: INSTRUMENT, ULTRASONIC SURGICAL
• Manufacturer (Section D): STRYKER INSTRUMENTS-INAGI; 1131-1 higashi naganuma; inagi 206-0 802
• MDR Report Key: 8546070
• Report Number: 0008043928-2019-00005
• Device Sequence Number: 1993224
• Product Code: LFL
• UDI-Device Identifier: 07613327291933
• UDI-Public: 07613327291933
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Number of Events Summarized: 3
• Summary Report (Y/N): Y
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/26/2019

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: No Information
• Device Catalogue Number: 5450840000
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 01/01/2019
• Supplement Date Received by Manufacturer: 01/01/2019
• Initial Report FDA Received Date: 04/24/2019
• Supplement Report FDA Received Date: 07/26/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1