MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US GLEN MANUAL REAMER D42 MM; EXTREMITY INSTRUMENTS : REAMERS

Model Number	2307-88-242
Medical Device Problem Code	Failure to Cut (2587)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/14/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Product complaint # (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
It was reported that this was a procedure treating reverse shoulder arthroplasty on (b)(6) 2021.The surgeon used the reamers for scraping the bone.Since the reamers were not sharp enough, the surgeon had difficulty in scraping the bone.No surgical delay.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary = the device associated with this report was not returned for evaluation.The investigation could not draw any conclusions about the reported event without the device to examine.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot =a manufacturing records evaluation (mre) was not performed as no lot number was provided for this device.

• Brand Name: GLEN MANUAL REAMER D42 MM
• Common Device Name: EXTREMITY INSTRUMENTS : REAMERS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 12239431
• Report Number: 1818910-2021-16305
• Device Sequence Number: 14413358
• Product Code: HTO
• UDI-Device Identifier: 10603295116486
• UDI-Public: 10603295116486
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• 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
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 07/13/2021

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: 2307-88-242
• Device Catalogue Number: 230788242
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 07/13/2021
• Supplement Date Received by Manufacturer: 10/05/2021
• Initial Report FDA Received Date: 07/28/2021
• Supplement Report FDA Received Date: 10/06/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1