FDA Adverse Event Injury Summary report: N

SROM STM ST,36+6L NK,11X16X150

MDR report key: 5567620 · Received April 11, 2016

Report

Report Number
1818910-2016-17098
Event Type
Injury
Date Received
April 11, 2016
Date of Event
April 5, 2016
Report Date
April 7, 2016
Manufacturer
DEPUY IRELAND ¿ REG. # 9616671
Product Code
LPH
PMA / PMN Number
PK954935
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. (B)(4).

Additional Manufacturer Narrative · 1

ADDITIONAL NARRATIVE: CLINICAL REPORT STATES THAT PATIENT EXPERIENCED AN INTRAOPERATIVE FEMORAL BONE FRACTURE. NO DEVICES WERE RETURNED FOR REVIEW. ONE OTHER REPORT FOUND AGAINST THE 8230706 LOT CODE. REVIEW OF DEVICE HISTORY RECORDS FINDS NO RELATED MANUFACTURING DEVIATIONS OR ANOMALIES THAT WOULD HAVE CONTRIBUTED TO THE REPORTED EVENT. NO OTHER REPORTS FOUND AGAINST THE REMAINING PRODUCT/LOT CODE COMBINATION. MEDICAL RECORDS AND X-RAYS WERE REVIEWED. THE INVESTIGATION CAN DRAW NO CONCLUSIONS WITH THE INFORMATION MADE AVAILABLE. BASED ON THE INABILITY TO DETERMINE A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION HAS NOT BEEN IDENTIFIED. DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Description of Event or Problem · 1

CLINICAL REPORT STATES THAT PATIENT EXPERIENCED AN INTRAOPERATIVE FEMORAL BONE FRACTURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
223686 SROM STM ST,36+6L NK,11X16X150 HIP FEMORAL STEM/SLEEVE LPH DEPUY IRELAND ¿ REG. # 9616671 8230706

Patients

Seq Age Sex Outcome Treatment
1 65 YR