FDA Adverse Event Injury Summary report: N

ANTIROTATION SCREW FOR FEMORAL NECK SYS 85MM LENGTH - STERILE

MDR report key: 9135267 · Received September 30, 2019

Report

Report Number
2939274-2019-61043
Event Type
Injury
Date Received
September 30, 2019
Report Date
September 4, 2019
Manufacturer
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
Product Code
KTT
UDI-DI
10886982274595
PMA / PMN Number
K000682
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. PRODUCT WAS NOT RETURNED. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

IT WAS REPORTED ON (B)(6) 2019, THE PATIENT PRESENTED IN THE CLINIC DUE TO POST-OPERATIVE PAIN ON THE HIP. AN X-RAY SHOWED NON-UNION WITH BROKEN ANTI-ROTATION SCREW AND POTENTIALLY THE BOLT IS BROKEN. THE DISTAL LOCKING SCREWS AND PLATE APPEAR TO BE INTACT. INITIALLY, THE PATIENT UNDERWENT AN OPEN REDUCTION INTERNAL FIXATION (ORIF) OF THE RIGHT FEMUR ON AN UNKNOWN DATE. AT THIS POINT, NO REVISION SURGERY HAS BEEN SCHEDULED. CONCOMITANT DEVICE REPORTED: TITANIUM LOCKING COMPRESSION PLATE (LCP) PROXIMAL LATERAL TIBIA (PART # 422.226, LOT # 2192572, QUANTITY 1). FEMORAL NECK SYSTEM PLATE (PART # 04.168.000S, LOT # UNKNOWN, QUANTITY 1). TITANIUM LOCKING SCREW (PART # 412.213S, LOT # UNKNOWN, QUANTITY 1) AND UNKNOWN LOCKING SCREWS (PART # UNKNOWN, LOT # UNKNOWN, QUANTITY UNKNOWN). THIS REPORT IS FOR ONE (1) ANTI-ROTATION SCREW FOR FEMORAL NECK SYS 85MM LENGTH - STERILE. THIS IS REPORT 1 OF 2 FOR (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
930741 ANTIROTATION SCREW FOR FEMORAL NECK SYS 85MM LENGTH - STERILE APPLIANCE, FIXATION, NAIL KTT WRIGHTS LANE SYNTHES USA PRODUCTS LLC 04.168.485S 10886982274595

Patients

Seq Age Sex Outcome Treatment
1 52 YR Required Intervention