MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US ADV+ CUTTING GUIDE CLAMP; EXTREMITY INSTRUMENTS : CLAMPS

Model Number	2128-62-150
Medical Device Problem Code	Mechanical Jam (2983)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/29/2021
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 when surgeon tried to use the humeral head resection guide, that adjustable plunger instrument would not let the cutting guide slide to the appropriate position, because the ball-bearing or spring pin inside the resection was frozen.Tried to loosen to allow adjustment, but did not succeed.Surgeon proceeded with the surgery by free-handing the humeral resection.It was also reported that only one instrument failed, the case was not delayed.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary : no device was received for examination, therefore the reported event could not be confirmed.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 : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.

• Brand Name: ADV+ CUTTING GUIDE CLAMP
• Common Device Name: EXTREMITY INSTRUMENTS : CLAMPS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 11828460
• Report Number: 1818910-2021-10379
• Device Sequence Number: 11839383
• Product Code: HXD
• UDI-Device Identifier: 10603295089858
• UDI-Public: 10603295089858
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/29/2021

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: 2128-62-150
• Device Catalogue Number: 212862150
• Device Lot Number: NW223496
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 04/29/2021
• Supplement Date Received by Manufacturer: 06/21/2021
• Initial Report FDA Received Date: 05/14/2021
• Supplement Report FDA Received Date: 06/22/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 60 YR