FDA Adverse Event Malfunction Summary report: N

DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA

MDR report key: 8951281 · Received August 30, 2019

Report

Report Number
2939274-2019-60252
Event Type
Malfunction
Date Received
August 30, 2019
Report Date
August 2, 2019
Manufacturer
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
Product Code
HTO
UDI-DI
10886982189042
PMA / PMN Number
K042899
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL PROCODES: NBH, HRX. MANUFACTURING LOCATION: SUPPLIER ¿ CRITERION TOOL & DIE / INSPECTED, PACKAGED AND RELEASED BY: (B)(4). RELEASE TO WAREHOUSE DATES: MAY 16, -2017 QUANTITY 15 / JUNE 05, 2017 QUANTITY (B)(4). PART: 314.743, DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA. LOT: H220887 (NON-STERILE). LOT QUANTITY: (B)(4). WORK ORDER TRAVELER MET ALL INSPECTION ACCEPTANCE CRITERIA. CERTIFICATES OF CONFORMANCE SUPPLIED BY CRITERION TOOL AND DIE WERE REVIEWED AND DETERMINED TO BE CONFORMING. NOTE: CERTIFICATES OF COMPLIANCE IDENTIFIES RAW MATERIAL TYPE(S) USED BUT DOES NOT PROVIDE ADDITIONAL CONFORMANCE / TEST REPORTS FOR SPECIFIC RAW MATERIALS. INSPECTION SHEETS, INCOMING FINAL INSPECTION MET ALL INSPECTION ACCEPTANCE CRITERIA APART FROM THE TWO PIECES NOTED. PACKAGING LABEL LOGS WERE REVIEWED AND DETERMINED TO BE CONFORMING. THIS LOT MET ALL DIMENSIONAL, VISUAL AND PACKAGING CRITERIA AT THE TIME OF RELEASE WITH NO ISSUES DOCUMENTED DURING THE INSPECTION OR RELEASE OF THE PRODUCT THAT WOULD CONTRIBUTE TO THIS COMPLAINT CONDITION. VISUAL INSPECTION: THE DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA WAS RETURNED AND RECEIVED AT US CUSTOMER QUALITY (CQ). UPON VISUAL INSPECTION, IT WAS OBSERVED THAT THE COUPLER DISTAL TIP OF THE DEVICE BROKEN. THE BROKEN OFF DISTAL TIP FRAGMENTS WERE NOT RECEIVED AT CQ. NO OTHER ISSUES WERE IDENTIFIED. THIS IS CONSISTENT WITH THE REPORTED COMPLAINT CONDITION, THUS CONFIRMING THE COMPLAINT. DIMENSIONAL INSPECTION: DIMENSIONAL INSPECTION OF THE RECEIVED DEVICE WAS PERFORMED AT CQ. OUTER DIAMETER OF THE DRIVE SHAFT WAS MEASURED TO BE WITHIN SPECIFICATION AS PER THE DRAWING. INNER DIAMETER OF THE DRIVE SHAFT WAS MEASURED TO BE WITHIN SPECIFICATION AS PER THE DRAWING. DOCUMENT/SPECIFICATION REVIEW: BASED ON THE DATE OF MANUFACTURE THE FOLLOWING DRAWINGS, REFLECTING THE CURRENT AND MANUFACTURED REVISION WERE REVIEWED: DRIVE SHAFT ASSEMBLY RIA, DRIVE SHAFT RIA. CONCLUSION: THE COMPLAINT CONDITION IS CONFIRMED FOR THE DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA AS THE DEVICE WAS BROKEN. THERE IS NO INDICATION THAT A DESIGN OR MANUFACTURING ISSUE HAS CAUSED THE BREAKAGE AND HENCE, THE ROOT CAUSE CANNOT BE DETERMINED. 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 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, DURING INSPECTION OF THE INSTRUMENTS BEFORE GOING THROUGH DECONTAMINATION PROCESS, A DRIVER SHAFT FOR REAMER IRRIGATOR ASPIRATOR (RIA) WAS DAMAGED. THE TIP WAS BROKEN OFF AND A DISPOSABLE REAMER TIP CANNOT BE PUT ON THE SHAFT. THERE WERE NO SURGICAL PROCEDURE AND PATIENT INVOLVEMENT. CONCOMITANT DEVICES: REAMER (PART: UNKNOWN, LOT: UNKNOWN, QUANTITY: 1). THIS REPORT IS FOR A DRIVE SHAFT-MINIMUM 520MM. THIS IS REPORT 1 OF 1 FOR (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
745165 DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA REAMER HTO WRIGHTS LANE SYNTHES USA PRODUCTS LLC 314.743 H220887 10886982189042

Patients

Seq Age Sex Outcome Treatment
1