MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS, INC. 1818910 LCS FEM A/P RESC GD STD; KNEE INSTRUMENT : RESECTION BLOCKS/DEVICES

Catalog Number	228733000
Medical Device Problem Code	Device-Device Incompatibility (2919)
Health Effect - Clinical Code	Not Applicable (3189)
Date of Event	10/15/2018
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
Upon using the resection block and rod, the surgeon found that the rod didn't fit through the resection block properly.
Additional Manufacturer Narrative
Product complaint #: (b)(4).Investigation summary: no devices were returned.Depuy synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation may 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: LCS FEM A/P RESC GD STD
• Common Device Name: KNEE INSTRUMENT : RESECTION BLOCKS/DEVICES
• Manufacturer (Section D): DEPUY ORTHOPAEDICS, INC. 1818910; 700 orthopaedic drive; warsaw IN 46582 0988
• MDR Report Key: 8029560
• Report Number: 1818910-2018-74227
• Device Sequence Number: 11144418
• Product Code: HAW
• UDI-Device Identifier: 10603295110088
• UDI-Public: 10603295110088
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K043223
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,o
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/14/2018

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: 228733000
• Device Lot Number: J0206
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 10/14/2018
• Supplement Date Received by Manufacturer: 12/20/2018
• Initial Report FDA Received Date: 11/01/2018
• Supplement Report FDA Received Date: 01/04/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1