MAUDE Adverse Event Report: STRYKER SPINE-FRANCE RELIANCE C DOUBLE SIDED RASP 7MM; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Catalog Number	48365207
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	09/28/2016
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that during an anterior cervical fusion a double sided rasp came apart while being from the patient 's neck.
Additional Manufacturer Narrative
Lot# 062182; visual inspection, device history review, complaint history review, risk assessment.The device was inspected and it was found that the handle was fractured.No relevant manufacturing issues were identified as all units met stryker specifications.Device was found to be more than 10 years old.The probable root cause of this event is determined to be normal wear and tear of instrument.
Event or Problem Description
It was reported that during an anterior cervical fusion a double sided rasp came apart while being from the patient 's neck.

• Brand Name: RELIANCE C DOUBLE SIDED RASP 7MM
• Common Device Name: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
• Manufacturer (Section D): STRYKER SPINE-FRANCE; zone industrielle de marticot; cestas 33610 ; FR 33610
• MDR Report Key: 6055243
• Report Number: 0009617544-2016-00424
• Device Sequence Number: 19022022
• Product Code: LXH
• UDI-Device Identifier: 07613327269888
• UDI-Public: (01)07613327269888
• Combination Product (Y/N): N
• Initial Reporter State: AR
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 01/13/2017

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: No Information
• Device Catalogue Number: 48365207
• Device Lot Number: 062182
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/18/2016
• Type of Report(Section G): FDA Requested
• Initial Date Received by Manufacturer: 09/28/2016
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 10/25/2016
• Supplement Report FDA Received Date: 01/13/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 34 YR