MAUDE Adverse Event Report: ZIMMER SURGICAL SA MOD ELEC/BATT DBL TRIG HP; BONE/JOINT SURGICAL POWER TOOL MOTOR, ELECTRIC

Model Number	N/A
Medical Device Problem Codes	Failure to Shut Off (2939); Physical Resistance/Sticking (4012)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/04/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).G2 ¿ foreign ¿ brazil.Investigation of this incident is currently ongoing.Once the investigation is completed, a supplemental medwatch 3500a will be submitted.
Event or Problem Description
It was reported that the trigger of the handpiece was sticking and when it was activated, the engine would not turn off.As a result, when the doctor began the technique to mill the acetabulum, the mill ended up wrapping around the scrub nurse's glove and coat, it ended up on the scrub nurse's wrist resulting in a superficial cut.Due diligence is in progress for this complaint; to date no additional information or product has been received.
Additional Manufacturer Narrative
Upon reassessment of the reported event, it was determined that this medwatch # (b)(4) is a duplicate of medwatch # (b)(4) which is reported under mfr 0008031000-2024-00163.Given this information, this medwatch will be voided.
Event or Problem Description
Upon reassessment of the reported event, it was determined this medwatch # (b)(4) is a duplicate of medwatch # (b)(4) which is reported under mfr 0008031000-2024-00163.Given this information, this medwatch will be voided.

• Brand Name: MOD ELEC/BATT DBL TRIG HP
• Common Device Name: BONE/JOINT SURGICAL POWER TOOL MOTOR, ELECTRIC
• Manufacturer (Section D): ZIMMER SURGICAL SA; 3, ch. du pre fleuri; 1228 plan-les-ouates; geneva CH-12 28; SZ CH-1228
• Manufacturer (Section G): ZIMMER SURGICAL SA; 3, ch. du pre fleuri; 1228 plan-les-ouates; geneva CH-12 28; SZ CH-1228
• Manufacturer Contact: christina arnt ; 56 e. bell drive; warsaw, IN 46582 ; 5745273773
• MDR Report Key: 20036665
• Report Number: 0008031000-2024-00145
• Device Sequence Number: 3075208
• Product Code: HAB
• UDI-Device Identifier: 00889024354593
• UDI-Public: (01)00889024354593
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Nurse
• Type of Report: Initial,Followup
• Report Date (Section B): 10/09/2024

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?: Yes
• Operator of Device: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 89-8507-400-00
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/23/2024
• Supplement Date Received by Manufacturer: 10/02/2024
• Initial Report FDA Received Date: 08/22/2024
• Supplement Report FDA Received Date: 10/09/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 74 YR
• Patient Sex: Female