MAUDE Adverse Event Report: DEPUY MITEK LLC US SUPER/RC DRBIT 2.9MM *EA; SURGICAL HAND DRILL

Catalog Number	211113
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Evaluation statement the product is not being returned, it has been discarded by the customer.We attribute the product's condition to fair wear & tear due to age and use as it is over 2 years old and has seen heavy use.No corrective action is required and no further action is warranted.Udi (b)(4) incomplete the lot number is currently unavailable.This report is being filed from the remetrex complaint management system as required under mitek's corrective and preventative actions (capa) to file usa fda mdr missed malfunctions.
Event or Problem Description
The inventory manager for arthrosource reported that while going through their equipment they found their super anchor drill bit had a broken tip.The manager verified that the device was not used in a procedure and there were no patient consequences.The inventory manager stated that the device was over 2 years old and had seen heavy use.The device was discarded.

• Common Device Name: SURGICAL HAND DRILL
• Manufacturer (Section D): DEPUY MITEK LLC US; 325 paramount drive; raynham MA 02767
• MDR Report Key: 7800144
• Report Number: 1221934-2018-50979
• Device Sequence Number: 19459890
• Product Code: HTW
• UDI-Device Identifier: 10886705001583
• UDI-Public: 10886705001583
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 05/09/2013

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: 211113
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/09/2013
• Initial Report FDA Received Date: 08/20/2018
• Patient Sequence Number: 1