FDA Adverse Event Malfunction Summary report: N

ALINITY C PROCESSING MODULE

MDR report key: 17452027 · Received August 3, 2023

Report

Report Number
3016438761-2023-00414
Event Type
Malfunction
Date Received
August 3, 2023
Date of Event
July 9, 2023
Report Date
November 9, 2023
Manufacturer
ABBOTT LABORATORIES
Product Code
JJE
UDI-DI
00380740137380
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE ALINITY C PROCESSING MODULE, SERIAL NUMBER (B)(6) WAS INSPECTED. IT WAS DISCOVERED THAT THE POWER ISSUE WAS COMING FROM SIO BOARD AND THAT THE CARRIER POSITIONER MOTOR ENCODER/HOME CABLE HAD SHORTED TO THE FRAME. NO FIRE OR SMOKE WAS SEEN NOR ANY DAMAGE OTHER PARTS OF THE INSTRUMENT. THE SIO BOARD AND THE CARRIER POSITIONER MOTOR ENCODER/HOME CABLE WERE REPLACED. RETURN TESTING WAS NOT COMPLETED AS RETURNS WERE NOT AVAILABLE. THE INSTRUMENT SERVICE HISTORY REVIEW REVEALED NO ADDITIONAL ISSUES RELATED TO THE REPORTED EVENT. A REVIEW OF TRACKING AND TRENDING DID NOT IDENTIFY A TREND FOR THE SIO BOARD OR THE CARRIER POSITIONER MOTOR ENCODER/HOME CABLE AND REVIEW FOUND NO SIMILAR ISSUES WITH REGARDS TO THE REPORTED ISSUE. A REVIEW OF THE MANUFACTURING DOCUMENTATION DID NOT IDENTIFY ANY NON-CONFORMANCES OR POTENTIAL NON-CONFORMANCES RELATED TO THE SIO BOARD OR THE CARRIER POSITIONER MOTOR ENCODER/HOME CABLE. A LABELING REVIEW DETERMINED PRODUCT LABELING ADDRESSES TROUBLESHOOTING AND PROVIDES RESOLUTION FOR THE REPORTED EVENT. THE 2023 UL CERTIFICATION MEMO INDICATES THAT ABBOTT DIAGNOSTIC EQUIPMENT AND ACCESSORIES ARE CERTIFIED TO THE APPROPRIATE SAFETY STANDARDS, AND ADEQUATE PROTECTION IS PROVIDED FOR THE OPERATOR AGAINST SPREAD OF FIRE FROM THE EQUIPMENT. THE SHORT-CIRCUITED PART OBSERVED, DUE TO THE POWER ISSUE COMING FROM SIO DRIVER BD WAS LIMITED TO THE CARRIER POSITIONER MOTOR ENCODER/HOME CABLE; THE SHORT-CIRCUIT ISSUE DID NOT SPREAD TO OTHER PARTS OF THE MODULE. NO FIRE OR SMOKE WAS SEEN NOR ANY DAMAGE OTHER PARTS OF THE INSTRUMENT. BASED ON THE AVAILABLE INFORMATION, NO SYSTEMIC ISSUE OR DEFICIENCY WAS IDENTIFIED FOR THE ALINITY C PROCESSING MODULE, SERIAL NUMBER (B)(6), SIO BOARD, OR THE CARRIER POSITIONER MOTOR ENCODER/HOME CABLE.

Additional Manufacturer Narrative · 0

ALL AVAILABLE PATIENT INFORMATION WAS INCLUDED. ADDITIONAL PATIENT DETAILS ARE NOT AVAILABLE. AN EVALUATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE EVALUATION IS COMPLETE.

Description of Event or Problem · 0

THE CUSTOMER REPORTED THAT THEY WERE HAVING TROUBLE WITH THE SAMPLE PIPETTOR ON THE ALINITY C PROCESSING MODULE AND COMMUNICATED THE FOLLOWING ERROR CODES OCCURRED, 5689 - SAMPLE PIPETTOR MOVEMENT RESTRICTED AND 9415 - PROCESSING MODULE C ERROR. IT WAS REPORTED THAT SPARKS WERE OBSERVED WHEN THE CHASSIS OF THE SAMPLE POSITIONER ENCODER TOUCHED THE FRAME OF THE INSTRUMENT. A PINCHED CABLE ON THE A1C WASH VALVE WAS DISCOVERED. THE A1C CABLE WAS FOUND TO BE SHORTED OUT. A SHORT WAS ALSO DISCOVERED IN CNN 9 AND THE SIO BOARD WAS REPLACED. NO FURTHER SPARKS WERE OBSERVED. THERE WAS NO REPORTED IMPACT TO PATIENT MANAGEMENT.

Description of Event or Problem · 0

THE CUSTOMER REPORTED THAT THEY WERE HAVING TROUBLE WITH THE SAMPLE PIPETTOR ON THE ALINITY C PROCESSING MODULE AND COMMUNICATED THE FOLLOWING ERROR CODES OCCURRED, 5689 - SAMPLE PIPETTOR MOVEMENT RESTRICTED AND 9415 - PROCESSING MODULE C ERROR. IT WAS REPORTED THAT SPARKS WERE OBSERVED WHEN THE CHASSIS OF THE SAMPLE POSITIONER ENCODER TOUCHED THE FRAME OF THE INSTRUMENT. A PINCHED CABLE ON THE A1C WASH VALVE WAS DISCOVERED. THE A1C CABLE WAS FOUND TO BE SHORTED OUT. A SHORT WAS ALSO DISCOVERED IN CNN 9 AND THE SIO BOARD WAS REPLACED. NO FURTHER SPARKS WERE OBSERVED. THERE WAS NO REPORTED IMPACT TO PATIENT MANAGEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1507454 ALINITY C PROCESSING MODULE ANALYZER, CHEMISTRY (PHOTOMETRIC, DISCRETE), FOR CLINICAL USE JJE ABBOTT LABORATORIES 00380740137380

Patients

Seq Age Sex Outcome Treatment
1 Unknown