MAUDE Adverse Event Report: STRYKER INSTRUMENTS-KALAMAZOO MINI CUTTING GUIDE; NEUROLOGICAL STEREOTAXIC INSTRUMENT

Catalog Number	6003-300-010
Medical Device Problem Codes	Break (1069); Fracture (1260)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	08/01/2018
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the device was found in the sterile processing department at the user facility with the head of the device broken off.No medical intervention and no adverse consequences were reported with this event.As this event was discovered during sterile processing, there was no known patient involvement and no known delay to a surgical procedure.
Additional Manufacturer Narrative
Device evaluation: follow-up report submitted to document device evaluation results.
Event or Problem Description
It was reported that the device was found in the sterile processing department at the user facility with the head of the device broken off.No medical intervention and no adverse consequences were reported with this event.As this event was discovered during sterile processing, there was no known patient involvement and no known delay to a surgical procedure.

• Brand Name: MINI CUTTING GUIDE
• Common Device Name: NEUROLOGICAL STEREOTAXIC INSTRUMENT
• Manufacturer (Section D): STRYKER INSTRUMENTS-KALAMAZOO; 4100 east milham avenue; kalamazoo MI 49001
• MDR Report Key: 7812665
• Report Number: 0001811755-2018-01612
• Device Sequence Number: 13509990
• Product Code: HAW
• UDI-Device Identifier: 04546540502094
• UDI-Public: 04546540502094
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K993239
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: user facility
• Initial Reporter Occupation: Nurse
• Type of Report: Initial,Followup
• Report Date (Section B): 12/12/2018

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: 6003-300-010
• Device Lot Number: A/09/2011
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/31/2018
• Initial Date Received by Manufacturer: 08/01/2018
• Supplement Date Received by Manufacturer: 12/12/2018
• Initial Report FDA Received Date: 08/24/2018
• Supplement Report FDA Received Date: 12/12/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1