FDA Adverse Event Malfunction Summary report: N

ACCESS

MDR report key: 3830523 · Received May 23, 2014

Report

Report Number
1416980-2014-16819
Event Type
Malfunction
Date Received
May 23, 2014
Report Date
May 1, 2014
Manufacturer
BAXTER HEALTHCARE - HAINA, SAN CRISTOBAL
Product Code
FPA
PMA / PMN Number
K123874
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE SAMPLE WAS NOT RETURNED FOR EVALUATION, THEREFORE THE REPORTED CONDITION COULD NOT BE VERIFIED AND THE CAUSE COULD NOT BE IDENTIFIED. A BATCH REVIEW WAS CONDUCTED AND THERE WERE NO DEVIATIONS FOUND RELATED TO THIS REPORTED CONDITION DURING THE MANUFACTURE OF THIS LOT. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). A SAMPLE OF PRODUCT CODE (B)(4) WAS NOT RECEIVED. THE SAMPLE RECEIVED WAS OF A DIFFERENT PRODUCT CODE AND WILL BE CAPTURED AND REPORTED IN (B)(4). UPON COMPLETION OF BAXTER'S INVESTIGATION, IF ADDITIONAL RELEVANT INFORMATION IS OBTAINED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE HAS BEEN RECEIVED AND THE EVALUATION IS UNDERWAY. UPON COMPLETION OF BAXTER'S INVESTIGATION, IF ADDITIONAL RELEVANT INFORMATION IS OBTAINED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

A CUSTOMER REPORTED THAT THEIR INTERLINK BURETROL ADMINISTRATION SET WAS "FALLING APART" AND THAT THE CHAMBER APPEARED "CROOKED". IT IS UNKNOWN WHETHER THERE WAS PATIENT INVOLVEMENT OR PATIENT IMPACT ASSOCIATED WITH THIS REPORT, THOUGH NO INJURY OR MEDICAL INTERVENTION WAS REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
308112 ACCESS SET, ADMINISTRATION, INTRAVASCULAR FPA BAXTER HEALTHCARE - HAINA, SAN CRISTOBAL DR13L03039

Patients

Seq Age Sex Outcome Treatment
1