MAUDE Adverse Event Report: DEPUY IRELAND 9616671 ATTUNE CONV RP PS TB TRL SZ5; ATTUNE INSTRUMENTS : TIBIAL TRIALS

Catalog Number	254500995
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	06/25/2018
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
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
Attune total knee replacement.(b)(6): (b)(6) hospital, (b)(6) 2018.The spring on the size 5 attune ps rp insert trial broke during removal of the instrument following a trial reduction.All affected parts were accounted for, and the broken spring was discarded by the scrub nurse.Instrument was no longer needed, so operation continued as normal.No ae to patient.No delay to the procedure.Patient initial (b)(6).
Additional Manufacturer Narrative
Investigation summary the device associated with this report was not returned to depuy synthes in warsaw 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.If information is obtained that was not available for the initial medwatch , a follow-up medwatch, a follow-up medwatch will be filed as appropriate. .

• Brand Name: ATTUNE CONV RP PS TB TRL SZ5
• Common Device Name: ATTUNE INSTRUMENTS : TIBIAL TRIALS
• Manufacturer (Section D): DEPUY IRELAND 9616671; loughbeg, ringaskiddy co.; cork ; EI
• MDR Report Key: 7703407
• Report Number: 1818910-2018-64818
• Device Sequence Number: 906673
• Product Code: JWH
• UDI-Device Identifier: 10603295135722
• UDI-Public: 10603295135722
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K140881
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/25/2018

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 Catalogue Number: 254500995
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/25/2018
• Supplement Date Received by Manufacturer: 09/26/2018
• Initial Report FDA Received Date: 07/19/2018
• Supplement Report FDA Received Date: 09/27/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1