FDA Adverse Event Malfunction Summary report: N

HEMASHIELD WOVEN DOUBLE VELOUR FABRIC

MDR report key: 20492822 · Received October 21, 2024

Report

Report Number
1640201-2024-0000016
Event Type
Malfunction
Date Received
October 21, 2024
Date of Event
September 21, 2024
Report Date
December 11, 2024
Manufacturer
INTERVASCULAR SAS
Product Code
DXZ
UDI-DI
00384401018810
PMA / PMN Number
K955349
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(10/3233) THE INVOLVED DEVICE WAS RETURNED TO INTERVASCULAR FOR EXAMINATION. A VISUAL INSPECTION OF DEVICE WILL BE PERFORMED. (4101/3233) EIGHT OTHER DEVICES FROM THE SAME LOT NUMBER 24F19 WERE RETURNED FROM THE CUSTOMER AND WILL UNDERGO A VISUAL INSPECTION. (11/213) TWO RETENTION SAMPLES WERE SELECTED FROM THE SAME STERILIZATION LOT NUMBER WITH THE SAME FABRIC TYPE (WOVEN) AND THE SAME COATING PARAMETERS AS THE INVOLVED PRODUCT. A VISUAL INSPECTION OF THE RETENTION SAMPLES WAS PERFORMED BY A QUALIFIED QUALITY CONTROL TECHNICIAN AND THE TEAM MANAGER. IT WAS CONCLUDED THAT THE SAMPLES ARE IN COMPLIANCE WITH THE PRODUCT SPECIFICATIONS. (11) THE INVESTIGATION IS STILL ONGOING. A FOLLOW UP REPORT WILL BE SENT UPON COMPLETION OF THE INVESTIGATION.

Additional Manufacturer Narrative · 0

(10/4101/213) THE INVOLVED DEVICE WAS RETURNED TO INTERVASCULAR. A VISUAL INSPECTION WAS PERFORMED BY THE TEAM LEAD OF QUALITY CONTROL, PRODUCTION SUPERVISOR AND THE QUALITY ASSURANCE SUPERVISOR. THE INSPECTION RESULTS ARE THE FOLLOWING: 2 OUT OF 9 PATCHES ((B)(6)) WERE RECEIVED OPENED. THE OPENED PRODUCTS WERE INSPECTED AND SHOWED SLIGHT YELLOW AND SHINY COLLAGEN MARKS WITHOUT THICKENING. IT WAS CONCLUDED THAT THE INSPECTED DEVICES ARE CONFORM TO THE PRODUCT SPECIFICATIONS. (4109/213) THE REVIEW OF HISTORICAL DATA INDICATED THAT ANOTHER SIMILAR COMPLAINT ((B)(4), MFG EMDR #1640201-2024-0000027) ABOUT STAIN ON THE PATCH FOR LOT NUMBER 24F19 WAS REPORTED BY THE SAME CUSTOMER ON A DIFFERENT DATE. THE INVESTIGATION OF COMPLAINT (B)(4) CONCLUDED THAT THE PRODUCT IS IN COMPLIANCE WITH THE PRODUCT SPECIFICATIONS. (67) THE CONDUCTED INVESTIGATION CONCLUDES THAT THE RETURNED PRODUCT IS IN COMPLIANCE WITH THE PRODUCT SPECIFICATIONS.

Additional Manufacturer Narrative · 0

(10/3233) IT WAS REPORTED THAT THE PRODUCT IS AVAILABLE FOR INVESTIGATION, IT SHOULD BE RETURNED TO INTERVASCULAR FOR EXAMINATION. (4101/3233) EIGHT OTHER DEVICES FROM THE SAME LOT NUMBER 24F19 WILL BE RETURNED FROM THE CUSTOMER AND WILL UNDERGO A VISUAL INSPECTION. (4109/3233) THE REVIEW OF HISTORICAL DATA INDICATED THAT ONE OTHER SIMILAR COMPLAINT ( (B)(4) ) WAS REPORTED BY THE SAME CUSTOMER, INVOLVING ANOTHER PRODUCT WITH SAME PRODUCT REFERENCE AND FROM THE SAME LOT NUMBER 24F19. THE INVESTIGATION IS STILL ONGOING. (11/3233) TWO RETENTION SAMPLES WERE SELECTED FROM THE SAME STERILIZATION LOT NUMBER WITH THE SAME FABRIC TYPE (WOVEN) AND THE SAME COATING PARAMETERS AS THE INVOLVED PRODUCT. A VISUAL INSPECTION OF THE RETENTION SAMPLES IS ONGOING. (11) THE INVESTIGATION IS STILL ONGOING. A FOLLOW-UP REPORT WILL BE SENT UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 0

COMPLAINT #(B)(4).

Description of Event or Problem · 0

COMPLAINT #(B)(4).

Description of Event or Problem · 0

IT WAS REPORTED TO INTERVASCULAR THAT IT WAS NOTICED WATER MARKS ON A HEMASHIELD PATCH WITH REF. (B)(4) AND LOT NUMBER 24F19 PRIOR TO USING IT ON A PATIENT. NO HARM ON THE PATIENT AND NO ADDITIONAL TIME ADDED TO THE PROCEDURE WERE REPORTED. SUBSEQUENTLY, ANOTHER PATCH WITH THE SAME PRODUCT REFERENCE AND LOT NUMBER WAS PULLED FROM THE SHELF, AND WATER MARKS WERE OBSERVED BEFORE IT WAS REMOVED FROM THE STERILE PACKAGE. A TOTAL OF 9 HEMASHIELD PATCHES WITH THE SAME REFERENCE ( (B)(4) ) AND LOT NUMBER (24F19) WERE PULLED FROM THE SHELF. IT SHOULD BE NOTED THAT THIS EMDR IS PART OF A SERIE OF 9 EMDRS INVOLVING 9 HEMASHIELD PATCHES WITH DIFFERENT SERIAL NUMBERS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2220497 HEMASHIELD WOVEN DOUBLE VELOUR FABRIC PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE DXZ INTERVASCULAR SAS M002000196240 24F19 00384401018810

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown