FDA Adverse Event Malfunction Summary report: N

BD PLASTIPAK¿ LUER-LOK¿ SYRINGE

MDR report key: 16686958 · Received April 5, 2023

Report

Report Number
3003152976-2023-00118
Event Type
Malfunction
Date Received
April 5, 2023
Date of Event
March 17, 2023
Report Date
May 3, 2023
Manufacturer
BECTON DICKINSON, S.A.
Product Code
FMF
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DEVICE EVALUATED BY MFR: A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

H6: INVESTIGATION SUMMARY NO SAMPLES OR PICTURES RECEIVED FOR INVESTIGATION. A DEVICE HISTORY REVIEW WAS PERFORMED FOR THE REPORTED LOT 2112042 NO DEVIATIONS OR NON-CONFORMANCES WERE IDENTIFIED DURING THE MANUFACTURING PROCESS THAT COULD HAVE CONTRIBUTED TO THIS ISSUE. MANUFACTURING FOR THIS PRODUCT IS PERFORMED IN A CLEAN ROOM WHICH IS KEPT UNDER A POSITIVE PRESSURE TO REDUCE THE CHANCE OF FOREIGN MATTER. THE ASSEMBLY STATION HAS A DE-IONIZER AND VACUUM SYSTEM USED TO REMOVE ANY PARTICLES INSIDE THE BARREL. FINAL PRODUCTS IN THIS MANUFACTURING LINE, FOR THIS REFERENCE ARE SAMPLED AND THEY ARE SUBJECTED TO VISUAL AND FUNCTIONAL INSPECTIONS DURING THE DIFFERENT MANUFACTURING SUB-PROCESSES ACCORDING TO PROCEDURES. THE AREAS WHERE PIECES RUN IN MANUFACTURING AREA ARE PROTECTED TO AVOID DAMAGE ON THE PRODUCT AND REDUCE PARTICLES FROM GENERATING. WHILE WE CANNOT IDENTIFY A DIRECT ISSUE, POSSIBLE ROOT CAUSE IS HUMAN ERROR. H3 OTHER TEXT : SEE H10.

Description of Event or Problem · 0

IT WAS REPORTED THAT A HAIR WAS SEALED IN THE BD PLASTIPAK¿ LUER-LOK¿ SYRINGE STERILE PACKAGING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT HAS BEEN FOUND WITHIN OUR PERIOPERATIVE DEPARTMENT THAT A HAIR HAS BEEN SEALED WITHIN THE STERILE PACKAGING OF A 20ML LUER LOK SYRINGE."

Description of Event or Problem · 0

IT WAS REPORTED THAT A HAIR WAS SEALED IN THE BD PLASTIPAK¿ LUER-LOK¿ SYRINGE STERILE PACKAGING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT HAS BEEN FOUND WITHIN OUR PERIOPERATIVE DEPARTMENT THAT A HAIR HAS BEEN SEALED WITHIN THE STERILE PACKAGING OF A 20ML LUER LOK SYRINGE."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1820263 BD PLASTIPAK¿ LUER-LOK¿ SYRINGE PISTON SYRINGE FMF BECTON DICKINSON, S.A. 2112042

Patients

Seq Age Sex Outcome Treatment
1 Unknown