MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US AB EXTRACTOR BODY 58MM; HIP INSTRUMENTS : EXTRACTION INSTRUMENTS

Catalog Number	221700058
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	03/01/2017
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
This instrument complaint is linked to revision surgery (b)(4).(b)(6) hospital - (b)(6) 2018.Ab extractor lug broke when attempting to remove ceramic liner.Device ineffective in removal.Ceramic removed via alternative means.Hip revised.No patient issue relating to product issue.
Additional Manufacturer Narrative
Product complaint #: (b)(4).
Additional Manufacturer Narrative
(b)(4).Investigation summary: the instrument associated with this report was not returned.Depuy 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.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: AB EXTRACTOR BODY 58MM
• Common Device Name: HIP INSTRUMENTS : EXTRACTION INSTRUMENTS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46582 0988
• MDR Report Key: 7365201
• Report Number: 1818910-2018-55959
• Device Sequence Number: 1124713
• Product Code: HWB
• UDI-Device Identifier: 10603295097310
• UDI-Public: 10603295097310
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Health Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/01/2018

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: 221700058
• Device Lot Number: AH1103
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 03/01/2018
• Supplement Date Received by Manufacturer: 03/01/2018; 11/26/2018
• Initial Report FDA Received Date: 03/23/2018
• Supplement Report FDA Received Date: 03/23/2018; 11/27/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1