MAUDE Adverse Event Report: STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP SYSTEM 7 DUAL TRIGGER ROTARY HANDPIECE; INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Model Number 7205000000

Device Problem Fail-Safe Problem (2936)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 01/01/2021

Event Type  malfunction  

Manufacturer Narrative

This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events: 7 events were reported for this quarter.Product return status: 1 device was received.6 device investigation types have not yet been determined.7 devices were not labeled for single-use.7 devices were not reprocessed or reused.

Event Description

This report summarizes 7 malfunction events in which the device experienced a fail-safe problem that could result in unintended activation.7 events had no patient involvement; no patient impact.

Event Description

This report summarizes 7 malfunction events in which the device experienced a fail-safe problem that could result in unintended activation.- 7 events had no patient involvement; no patient impact.

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: h10.7 previously reported events are included in this follow-up record.Product return status.7 devices were received.

• Brand Name: SYSTEM 7 DUAL TRIGGER ROTARY HANDPIECE
• Type of Device: INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT
• Manufacturer (Section D): STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP; 1941 stryker way; portage MI 49002
• MDR Report Key: 11729060
• MDR Text Key: 247493431
• Report Number: 3015967359-2021-00672
• Device Sequence Number: 1
• Product Code: HWE
• UDI-Device Identifier: 07613252251002
• UDI-Public: 07613252251002
• Combination Product (y/n): N
• Number of Events Reported: 7
• Summary Report (Y/N): Y
• Report Source: Manufacturer
• Source Type: company representative
• Type of Report: Initial,Followup
• Report Date: 07/29/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 04/26/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Model Number: 7205000000
• Device Catalogue Number: 7205000000
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 01/01/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1