FDA Adverse Event Malfunction Summary report: N

COMPOUNDERS

MDR report key: 2165030 · Received July 17, 2011

Report

Report Number
6000001-2011-12495
Event Type
Malfunction
Date Received
July 17, 2011
Date of Event
June 28, 2011
Report Date
June 28, 2011
Manufacturer
BAXTER HEALTHCARE - BUFFALO GROVE
Product Code
NEP
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS DEVICE IS EXEMPT FROM HAVING A 510(K) NUMBER. HOWEVER, THIS PRODUCT IS BEING REPORTED BECAUSE IT IS SAME AS OR SIMILAR TO A PRODUCT DISTRIBUTED WITHIN THE U.S. ITS ADDITIONAL 510(K) NUMBER IS K961008. THE DEVICE IS AVAILABLE FOR EVALUATION PER THE CUSTOMER; HOWEVER, THE DEVICE HAS NOT YET BEEN RECEIVED BY BAXTER. SHOULD THE DEVICE BE RECEIVED BY BAXTER FOR EVALUATION, A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF AN EVALUATION OR IF ANY ADDITIONAL INFORMATION BECOMES AVAILABLE.

Additional Manufacturer Narrative · 1

(B)(4). AFTER FURTHER INVESTIGATION, THERE IS NO INFORMATION TO SUGGEST THAT THIS DEVICE MALFUNCTION WOULD CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY IF IT WERE TO RECUR.

Description of Event or Problem · 1

BAXTER RECEIVED A REPORT THAT AN AUTOMIX 3+3/AS COMPOUNDER HAD AN INCORRECT SOLUTION 2 MESSAGE. THIS CONDITION OCCURRED DURING COMPOUNDING IN THE PHARMACY AND WAS REPORTED TO HAVE OCCURRED MULTIPLE TIMES SINCE THE FACILITY RECEIVED THE DEVICE. THIS CONDITION CAN LEAD TO INCORRECT COMPOUNDING OR INCORRECT LABELING OF COMPOUNDING MATERIAL. THERE WAS NO PATIENT INVOLVEMENT; THEREFORE, NO PATIENT INJURY, MEDICAL INTERVENTION, OR ADVERSE REACTION IS ASSOCIATED WITH THE REPORTED CONDITION. THE SAMPLE IS AVAILABLE. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COMPOUNDERS SYSTEM/DEVICE, PHARMACY COMPOUNDING NEP BAXTER HEALTHCARE - BUFFALO GROVE

Patients

Seq Age Sex Outcome Treatment
1