MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US ANTEVERSION OSTEOTOME MED; HIP INSTRUMENTS : CUTTING INSTRUMENTS

Model Number	2002-25-000
Medical Device Problem Code	Failure to Cut (2587)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/01/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
Surgeon used two box osteotomes during a hemiarthoplasty case (one small and one medium) and both were dull and difficult to insert into bone.During the same case we also had an issue with the corail standard neck segment trial as it was very challenging to attach to any broach.I also tested after the case with the kho and kla neck trials and they attached very smoothly.No surgical or patient issues and no surgical delay.Case was completed successfully.No further information is available.
Additional Manufacturer Narrative
Product complaint # : (b)(4).Investigation summary : the instrument associated with this report was not returned.Depuy-synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed, and the investigation will be re-opened as necessary.Device history lot : a manufacturing record evaluation (mre), was not possible because the required lot code was not provided.

• Brand Name: ANTEVERSION OSTEOTOME MED
• Common Device Name: HIP INSTRUMENTS : CUTTING INSTRUMENTS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 11983764
• Report Number: 1818910-2021-12458
• Device Sequence Number: 14642667
• Product Code: HWM
• UDI-Device Identifier: 10603295080770
• UDI-Public: 10603295080770
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/01/2021

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 Number: 2002-25-000
• Device Catalogue Number: 200225000
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/01/2021
• Supplement Date Received by Manufacturer: 08/19/2021
• Initial Report FDA Received Date: 06/11/2021
• Supplement Report FDA Received Date: 08/19/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1