FDA Adverse Event Malfunction Summary report: N

UNKNOWN

MDR report key: 11270421 · Received February 2, 2021

Report

Report Number
3008258694-2021-00005
Event Type
Malfunction
Date Received
February 2, 2021
Date of Event
October 9, 2020
Report Date
February 1, 2021
Manufacturer
COMBAT MEDICAL SYSTEMS LLC
Product Code
POQ
Removal / Correction Number
300825869422DEC2020R001
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THIS WAS IDENTIFIED AT A TRAINING OPERATION WITHIN THE US MILITARY. NO PATIENT INVOLVEMENT. REFERENCE MDR NO. 3008258694-2021-00001. INITIAL MDR ASSESSMENT WAS COMPLETED AND DETERMINED NOT TO BE REPORTABLE BASED ON CUSTOMER USAGE (TRAINING EXERCISE) AND NO PATIENT IMPACT. HOWEVER, A FIELD ACTION WAS INITIATED AND IN AN ABUNDANCE OF CAUTION WE REEVALUATED OUR MDR ASSESSMENT AND ARE FILING THIS REPORT. COMBAT MEDICAL RECEIVED A COMPLAINT THAT THE BLOOD PACK NEEDLE WERE FOUND BENT UPON OPENING THE CONVENIENCE KIT. THE ISSUE WAS DISCOVERED TO BE ONE COMPONENT (A STAND ALONE DEVICE) WITHIN THE CONVENIENCE KIT: BLOOD PACK, SINGLE UNIT, R80-808. INVESTIGATION HAS SHOWN THAT THE CURRENT ASSEMBLY PROCESS HAS THE POTENTIAL OF BENDING/DISCONNECTING THE NEEDLES USED IN THE AFFECTED KITS. THE INFLUENCE OF THE VARIATION OF THE NEEDLE POSITION WITHIN THE COMPONENT (BLOOD PACK, SINGLE UNIT, 450 ML (R80-808)), COUPLED WITH THE MANUAL ASSEMBLY PROCESS OF FOLDING THE BLOOD PACK IS CAUSING NEEDLE DAMAGE IN THE FINISHED PRODUCT.

Description of Event or Problem · 1

KIT COMPONENT, BLOOD PACK 450ML LOT NUMBER FM20E27024, HAD A BENT NEEDLE WHEN KIT WAS OPENED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
167097 UNKNOWN CONVENIENCE KIT POQ COMBAT MEDICAL SYSTEMS LLC UNK

Patients

Seq Age Sex Outcome Treatment
1 Other