POLY SCW DRIVER SHFT, CANNULTD
Report
- Report Number
- 1526439-2020-01295
- Event Type
- Malfunction
- Date Received
- July 2, 2020
- Report Date
- March 25, 2020
- Manufacturer
- DEPUY SPINE INC
- Product Code
- HWR
- UDI-DI
- 10705034214177
- PMA / PMN Number
- EXEMPT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH DEPUY SYNTHES HAS NOT BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY FDA, DEPUY SYNTHES OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE DEVICE, DEPUY SYNTHES, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. 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.
OCCUPATION: REPORTER IS A SALES REPRESENTATIVE. A PRODUCT INVESTIGATION WAS CONDUCTED. VISUAL INSPECTION: THE POLY SCW DRIVER SHFT, CANNULTD (PART # 286720000 / LOT # UI0412 ) WAS RECEIVED AT US CQ. THE DISTAL TIP OF THE DEVICE WAS BROKEN, NO FRAGMENTS WERE RETURNED. THERE WERE SURFACE SCRATCHES AND NICKS CONSISTENT WITH NORMAL WEAR ALONG THE SHAFT OF THE DEVICE. THE RECEIVED CONDITION WAS CONSISTENT WITH THE COMPLAINT CONDITION THUS THE COMPLAINT WAS CONFIRMED. DIMENSIONAL INSPECTION: SINCE THE DISTAL TIP WAS BROKEN, THE DIAMETER OF THE SHAFT ADJACENT TO BREAKAGE WAS MEASURED PER RELEVANT DRAWING. TIP DIAMETER WAS MEASURED AND FOUND TO BE CONFORMING. DOCUMENT/SPECIFICATION REVIEW: RELEVANT DRAWING(S) REVIEWED. CONCLUSION: THE OVERALL COMPLAINT WAS CONFIRMED FOR THE RECEIVED POLY SCW DRIVER SHFT, CANNULTD (PART # 286720000 / LOT # UI0412 ) AS THE DISTAL TIP OF THE DEVICE WAS BROKEN. ALTHOUGH NO DEFINITIVE ROOT-CAUSE CAN BE DETERMINED IT IS POSSIBLE THE DEVICE EXPERIENCED UNINTENDED FORCES LEADING TO THE BREAKAGE. THERE WAS NO INDICATION THAT A DESIGN OR MANUFACTURING ISSUE CONTRIBUTED TO THE COMPLAINT. NO DESIGN ISSUES WERE OBSERVED DURING THE DOCUMENT/SPECIFICATION REVIEW. BASED ON THE INVESTIGATION FINDINGS, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. ADDITIONAL MONITORING FOR ANY POTENTIAL SAFETY SIGNALS WILL BE CONDUCTED THROUGH COMPLAINT TRENDING AND OTHER POST MARKET SAFETY SURVEILLANCE ACTIVITIES. A DEVICE HISTORY RECORD (DHR) REVIEW WAS CONDUCTED: A REVIEW OF THE RECEIVING INSPECTION (RI) FOR POLY SCW DRIVER SHFT, CANNULTD WAS CONDUCTED IDENTIFYING THAT LOT NUMBER UI0412 WAS RELEASED IN A SINGLE BATCH. BATCH 1: LOT QTY OF UI0412 UNITS WERE RELEASED ON 30JUN2012 WITH NO DISCREPANCIES. AS A RESULT, THE RI IDENTIFIED NO ISSUES DURING THE MANUFACTURING AND RELEASE OF THIS DEVICE THAT COULD HAVE CONTRIBUTED TO THE PROBLEM REPORTED BY THE CUSTOMER. 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.
IT WAS REPORTED THAT ON UNKNOWN DATE, DURING THEIR OWN AUDIT OF THE SETS, DEVICES WERE ALL FOUND TO BE NON FUNCTIONAL AND BROKEN. UNFORTUNATELY NONE OF THEM ARE ASSOCIATED WITH ANY SPECIFIC CASE. THE DEVICES INVOLVED WERE VIPER POLYAXIAL DRIVERS, T20 DRIVER, FINAL TIGHTENER, SET SCREW INSERTER, AND ALSO SOME SKYLINE SCREW DRIVERS. THERE IS NO PATIENT INVOLVEMENT. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICES IT WAS IDENTIFIED THAT THE DISTAL TIP OF THE POLY SCREWDRIVER SHAFT CANNULATED WAS BROKEN. THIS DEVICE CONDITION WAS REASSESSED AND DETERMINED AS REPORTABLE ON JUNE 24, 2020. THIS REPORT IS FOR ONE (1) POLY SCW DRIVER SHFT, CANNULTD THIS IS REPORT 4 OF 6 FOR COMPLAINT (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 689138 | POLY SCW DRIVER SHFT, CANNULTD | DRIVER | HWR | DEPUY SPINE INC | 286720000 | UI0412 | 10705034214177 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |