FDA Adverse Event Injury Summary report: N

VANTAGE

MDR report key: 8449441 · Received March 25, 2019

Report

Report Number
1038671-2019-00182
Event Type
Injury
Date Received
March 25, 2019
Report Date
January 13, 2020
Manufacturer
EXACTECH, INC.
Product Code
HSN
PMA / PMN Number
K152217
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

SECTION H10: (A1) PATIENT IDENTIFIER: (B)(6). (B2) OUTCOMES ATTRIBUTED TO ADVERSE EVENT : ADDED CHECK FOR HOSPITALIZATION - INITIAL OR PROLONGED. (B5) AS REPORTED, IN JAN OF 2019, THE 77 Y/O MALE PATIENT¿S RIGHT ANKLE WAS NOTED AS COLLAPSED BACK INTO VARUS ANGULATION. IT IS NOTED AS RESOLVED IN 09/09/2019. THE PATIENT WEIGHS180 LBS. AND HEIGHT IS 5¿4¿. THE INITIAL IMPLANT ON R ANKLE WAS ON (B)(6) 2018.THE PATIENT HAS A HISTORY OF OSTEOARTHRITIS, HEART DISEASE, DIABETES, PARKINSON¿S DISEASE, AND GALLBLADDER CANCER. THE PATIENT HAS ALSO RECEIVED CORTICOSTEROID INJECTIONS. THE PATIENT USES A CANE FOR AMBULATION AND HAS BEEN INSTRUCTED ON STRETCHING EXERCISES. THE CASE REPORT FORM INDICATES THIS EVENT IS POSSIBLY RELATED TO DEVICES AND POSSIBLY RELATED TO PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES. (D4) UNIQUE IDENTIFIER (UDI) #: (B)(4). (E3) OCCUPATION: PHYSICIAN. (G5) PMA/510(K)NUMBER: K152217. (H3) AS REPORTED, IN JAN OF 2019, THE 77 Y/O MALE PATIENT¿S THE ANKLE WAS NOTED AS COLLAPSED BACK INTO VARUS ANGULATION. IT IS NOTED AS RESOLVED IN 09/09/2019. THE PATIENT WEIGHS: 180 LBS. AND HEIGHT IS 5¿4¿. THE INITIAL IMPLANT ON R ANKLE WAS ON 08/24/2018.THE PATIENT HAS A HISTORY OF OSTEOARTHRITIS, HEART DISEASE, DIABETES, PARKINSON¿S DISEASE, AND GALLBLADDER CANCER. THE PATIENT HAS ALSO RECEIVED CORTICOSTEROID INJECTIONS. THE PATIENT USES A CANE FOR AMBULATION AND HAS BEEN INSTRUCTED ON STRETCHING EXERCISES. THE CASE REPORT FORM INDICATES THIS EVENT IS POSSIBLY RELATED TO DEVICES AND POSSIBLY RELATED TO PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES. ACCORDING TO IFU# (B)(4): PATIENTS SHOULD BE INSTRUCTED ON THE LIMITATIONS OF THE PROSTHESIS AND THE POSSIBILITY OF SUBSEQUENT SURGERY. THE PATIENT SHOULD BE CAUTIONED TO MONITOR ACTIVITIES AND PROTECT THE REPLACED JOINT FROM UNREASONABLE STRESSES AND FOLLOW THE WRITTEN INSTRUCTIONS OF THE PHYSICIAN WITH RESPECT TO FOLLOW-UP CARE AND TREATMENT. PATIENTS SHOULD BE WARNED TO PROTECT THE JOINT REPLACEMENT FROM UNREASONABLE STRESSES AND TO FOLLOW THE TREATING PHYSICIAN¿S INSTRUCTIONS, UNTIL ANTERIOR WOUND HEALING IS COMPLETE. THIS DEVICE IS USED FOR TREATMENT AND NOT DIAGNOSIS. UPON REVIEW OF THE AVAILABLE INFORMATION, THERE IS NO EVIDENCE THAT THIS IS A DEVICE RELATED PROBLEM AND NO ALLEGATION AGAINST THE DEVICE. IMPLANTATION OF A TOTAL JOINT COULD RESULT PAIN, INFECTION, LOOSENING OF TOTAL JOINT HARDWARE AND THE PATIENT SHOULD MONITOR THEIR ACTIVITY AND STRESSES TO THE OPERATED ANKLE. THE MOST LIKELY CAUSE OF THE REPORTED EVENT IS THE PATIENT¿S CONDITIONS. SECTION H11: CORRECTIONS MADE IN THE FOLLOWING SECTION(S): (G3) REPORT SOURCE: HEALTH PROFESSIONAL.

Description of Event or Problem · 0

AS REPORTED, IN JAN OF 2019, THE 77 Y/O MALE PATIENT¿S RIGHT ANKLE WAS NOTED AS COLLAPSED BACK INTO VARUS ANGULATION. IT IS NOTED AS RESOLVED IN 09/09/2019. THE PATIENT WEIGHS: 180 LBS. AND HEIGHT IS 5¿4¿. THE INITIAL IMPLANT ON R ANKLE WAS ON 08/24/2018. THE PATIENT HAS A HISTORY OF OSTEOARTHRITIS, HEART DISEASE, DIABETES, PARKINSON¿S DISEASE, AND GALLBLADDER CANCER. THE PATIENT HAS ALSO RECEIVED CORTICOSTEROID INJECTIONS. THE PATIENT USES A CANE FOR AMBULATION AND HAS BEEN INSTRUCTED ON STRETCHING EXERCISES. THE CASE REPORT FORM INDICATES THIS EVENT IS POSSIBLY RELATED TO DEVICES AND POSSIBLY RELATED TO PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES.

Additional Manufacturer Narrative · 1

PENDING EVALUATION.

Description of Event or Problem · 1

INDEX SURGERY: (B)(6) 2018. COLLAPSE OF ANKLE BACK INTO VARUS ANGULATION. THE CASE REPORT FORM INDICATES THIS EVENT IS POSSIBLY RELATED TO DEVICES AND POSSIBLY RELATED TO PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241438 VANTAGE TALAR IMPLANT SZ 2 RT HSN EXACTECH, INC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R