MAUDE Adverse Event Report: SMITH & NEPHEW, INC. LGN HOUSING RESECT COLLET S3-8; PROSTHESISKNEPATLLOFMOROTIBIALSMICONSTRAINDUNCMNTDPOROUSCOATDPOLYMERMTALPOLYMR

Model Number	71434424
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Injury (2348)
Date of Event	01/21/2020
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that during surgery, surgeon almost took his finger as collet popped off while he was reaming for the box.It is unknown if there was a delay or how the procedure was concluded.
Additional Manufacturer Narrative
The information received by the manufacturer has been re-evaluated for mdr reporting.The information states that event did not occur, therefore, it was determined that this case does not meet the threshold for reporting and is a non-reportable event.If further details are provided confirming the occurrence of a reportable event, our files will be updated accordingly and a further report submitted outlining both the event details and our investigations performed.

• Brand Name: LGN HOUSING RESECT COLLET S3-8
• Common Device Name: PROSTHESISKNEPATLLOFMOROTIBIALSMICONSTRAINDUNCMNTDPOROUSCOATDPOLYMERMTALPOLYMR
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 9647983
• Report Number: 1020279-2020-00414
• Device Sequence Number: 14180016
• Product Code: MBH
• UDI-Device Identifier: 03596010549327
• UDI-Public: 03596010549327
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K121393
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 03/04/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 71434424
• Device Catalogue Number: 71434424
• Device Lot Number: 18KCW1011
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/29/2020
• Initial Date Received by Manufacturer: 01/21/2020
• Supplement Date Received by Manufacturer: 03/02/2020
• Initial Report FDA Received Date: 01/30/2020
• Supplement Report FDA Received Date: 03/04/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention