FDA Adverse Event Malfunction Summary report: N

POLY SCW DRIVER SHFT, CANNULTD

MDR report key: 10626675 · Received October 5, 2020

Report

Report Number
1526439-2020-01878
Event Type
Malfunction
Date Received
October 5, 2020
Date of Event
September 10, 2020
Report Date
September 10, 2020
Manufacturer
MEDOS INTERNATIONAL SàRL CH
Product Code
HWR
UDI-DI
10705034388526
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

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. IF THE INFORMATION IS UNKNOWN, NOT AVAILABLE OR DOES NOT APPLY, THE SECTION/FIELD OF THE FORM IS LEFT BLANK. H10 ADDITIONAL NARRATIVE: CORRECTED DATA: D1, D2, D4, D10, H3, H6. UPDATED DATA: D10, H4. INVESTIGATION SUMMARY VISUAL INSPECTION: THE POLY SCW DRIVER SHFT, CANNULTD (PART # 286720000 / LOT # UI193487) 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. DEVICE FAILURE/DEFECT IDENTIFIED? YES; DISTAL TIP WAS BROKEN DIMENSIONAL INSPECTION: SINCE THE DISTAL TIP WAS BROKEN, THE DIAMETER OF THE SHAFT ADJACENT TO BREAKAGE WAS MEASURED. DRAWING(S) SPECIFIED DIMENSIONS: TIP DIAMETER MEASURED DIMENSIONS: TIP DIAMETER = CONFIRMING DEVICE(S) USED: CA148P DOCUMENT/SPECIFICATION REVIEW: DRAWING(S) REVIEWED: (CURRENT); (MANUFACTURED) CONCLUSION: THE OVERALL COMPLAINT WAS CONFIRMED FOR THE RECEIVED POLY SCW DRIVER SHFT, CANNULTD (PART # 286720000 / LOT # UI193487) 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. DEVICE HISTORY LOT A REVIEW OF THE RECEIVING INSPECTION (RI) FOR POLY SCW DRIVER SHFT, CANNULTD WAS CONDUCTED IDENTIFYING THAT LOT NUMBER UI193487 WAS RELEASED IN A SINGLE BATCH. - BATCH1: LOT WAS RELEASED ON MARCH 12, 2014 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 HISTORY REVIEW 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.

Additional Manufacturer Narrative · 1

WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. PRODUCT WAS NOT RETURNED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED. 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 THAT ON AN UNKNOWN DATE, AS THE SCRUB TECH WAS SETTING THE ROOM UP FOR THE CASE HE NOTICED THE DRIVER WAS MISSING THE TIP. THE DRIVER WAS REMOVED FROM THE FIELD. THERE WAS NO PROCEDURE OR PATIENT INVOLVEMENT. THIS REPORT IS FOR ONE (1) POLYAXIAL SCREW DRIVER SHAFT. THIS IS REPORT 1 OF 1 FOR (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1090478 POLY SCW DRIVER SHFT, CANNULTD DRIVER HWR MEDOS INTERNATIONAL SàRL CH 286720000N UI193487 10705034388526

Patients

Seq Age Sex Outcome Treatment
1