MAUDE Adverse Event Report: SMITH & NEPHEW, INC. INTERTAN 13MM X 42CM 130D RT; NAIL, FIXATION, BONE

Catalog Number	71675440
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	Injury (2348)
Date of Event	06/14/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported a revision surgery to remove the broken intertan nail and compression screw.
Additional Manufacturer Narrative
The associated complaint device was not returned.A review of complaint history did not reveal additional complaints for the listed batch.A review of the manufacturing records for the listed batch did not reveal a manufacturing abnormality that could have caused or contributed to the reported incident.The medical investigation concluded that no relevant supporting clinical information has been provided to assist with a clinical investigation.Therefore, based on insufficient information, a thorough clinical assessment cannot be performed at this time.Without the actual product involved, our investigation cannot proceed.If the device or new information is received in the future, the complaint can be re-opened.No further actions are being taken at this time.

• Brand Name: INTERTAN 13MM X 42CM 130D RT
• Common Device Name: NAIL, FIXATION, BONE
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 8756496
• Report Number: 1020279-2019-02603
• Device Sequence Number: 1488931
• Product Code: JDS
• UDI-Device Identifier: 00885556037867
• UDI-Public: 00885556037867
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K040212
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/09/2019

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 Expiration Date: 05/05/2019
• Device Catalogue Number: 71675440
• Device Lot Number: 09EM04693
• Initial Date Received by Manufacturer: 06/14/2019
• Supplement Date Received by Manufacturer: 10/03/2019
• Initial Report FDA Received Date: 07/03/2019
• Supplement Report FDA Received Date: 10/09/2019
• 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: Hospitalization; Required Intervention