MAUDE Adverse Event Report: STRYKER SPINE-FRANCE BLOCKER; PEDICLE SCREW SPINAL SYSTEM

Model Number	48850000
Medical Device Problem Code	Migration or Expulsion of Device (1395)
Health Effect - Clinical Codes	No Consequences Or Impact To Patient (2199); No Known Impact Or Consequence To Patient (2692)
Date of Event	06/01/2017
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that; patient complains of 'squeaking' coming from his lower back.
Additional Manufacturer Narrative
The customer reported event was confirmed via correspondence with the sales representative.Visual, dimensional and functional analysis could not be performed as the device was not returned.The device is still implanted.No lot # was provided, so a manufacturing record review could not be performed.The definitive root cause of the event cannot be determined from the given information.
Event or Problem Description
It was reported that; patient complains of 'squeaking' coming from his lower back.

• Brand Name: BLOCKER
• Common Device Name: PEDICLE SCREW SPINAL SYSTEM
• Manufacturer (Section D): STRYKER SPINE-FRANCE; zone industrielle de marticot; cestas 33610 ; FR 33610
• MDR Report Key: 6775568
• Report Number: 0009617544-2017-00310
• Device Sequence Number: 13838074
• Product Code: MNI
• UDI-Device Identifier: 07613327132526
• UDI-Public: (01)07613327132526
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/26/2017

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 Model Number: 48850000
• Device Catalogue Number: 48850000
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 07/12/2017
• Supplement Date Received by Manufacturer: 07/12/2017
• Initial Report FDA Received Date: 08/08/2017
• Supplement Report FDA Received Date: 10/26/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 40 YR