I-STAT ACT KAOLIN CARTRIDGE
Report
- Report Number
- 2245578-2026-00051
- Event Type
- Malfunction
- Date Received
- March 12, 2026
- Date of Event
- February 2, 2026
- Report Date
- March 12, 2026
- Manufacturer
- ABBOTT POINT OF CARE INC.
- Product Code
- JBP
- UDI-DI
- 10054749000156
- PMA / PMN Number
- K023582
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WI, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
APOC INCIDENT#: (B)(4). APOC LABELING WILL BE EVALUATED DURING THE INVESTIGATION AS PERTAINING TO THE EVENT.
ON 18-FEB-2026, ABBOTT POINT OF CARE WAS CONTACTED BY A CUSTOMER REGARDING I-STAT ACT KAOLIN CARTRIDGES THAT YIELDED A DISCREPANT RESULTS ON A PATIENT. THERE WAS NO PATIENT INFORMATION AVAILABLE. RETURN PRODUCT IS NOT AVAILABLE FOR INVESTIGATION. DATE: TESTED: RESULT (SECS) : ON (B)(6) 2026, 0911, 184, ON (B)(6) 2026, 0919, 179, ON (B)(6) 2026, 0934, 184, ON (B)(6) 2026, 1004, >1000, ON (B)(6) 2026, 1017, >1000, ON (B)(6) 2026, 1027, >1000, ON (B)(6) 2026, 1044, 179. THERE WAS NO HEPARIN TIME/DOSE INFORMATION. COLLECTED AND TESTED IMMEDIATELY. AT THIS TIME THERE IS NO REASON TO SUSPECT A MALFUNCTION EXISTS. THE REPORTING DECISION WAS BASED ON THE LIMITED INFORMATION AVAILABLE THAT SUGGESTS THE PRODUCT WAS NOT PERFORMING WITHIN THE VARIABILITY OF THE ASSAY. AN INVESTIGATION IS UNDERWAY. PER I-STAT SYSTEM MANUAL (ART: 714185-00Q), THE I-STAT KAOLIN ACTIVATED CLOTTING TIME (KAOLIN ACT) TEST IS AN IN VITRO DIAGNOSTIC TEST THAT USES FRESH, WHOLE BLOOD. AND IS USED TO MONITOR HIGH-DOSE HEPARIN ANTICOAGULATION FREQUENTLY ASSOCIATED WITH CARDIOVASCULAR SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 642226 | I-STAT ACT KAOLIN CARTRIDGE | ACT KAOLIN CARTRIDGE | JBP | ABBOTT POINT OF CARE INC. | NA | R25328 | 10054749000156 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |