ARCHITECT CREATINE KINASE
Report
- Report Number
- 1628664-2018-00332
- Event Type
- Malfunction
- Date Received
- July 21, 2018
- Report Date
- July 21, 2018
- Manufacturer
- ABBOTT MANUFACTURING INC
- Product Code
- CGS
- UDI-DI
- 00380740012878
- PMA / PMN Number
- K983070
- Removal / Correction Number
- 1628664-07/19/18-002-R
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SP
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
THE INITIAL MANUFACTURER REPORT WAS INADVERTENTLY MISSING THE 510K NUMBER, WHICH WAS ADDED TO SECTION PMA/510K (K983070). THERE ARE NO FURTHER UPDATES OR CHANGES.
A PRODUCT RECALL LETTER WAS ISSUED TO ALL ARCHITECT CUSTOMERS WHO HAVE RECEIVED ARCHITECT CREATINE KINASE, LIST NUMBER 07D63-21, LOT NUMBER 87697UN18. THE LETTER INFORMS THE CUSTOMER OF THE ISSUE REGARDING A STABILITY ISSUE THAT MAY LEAD TO QUALITY CONTROL RESULTS SHIFTING LOW OUT OF RANGE AND/OR ERROR CODE 1054 "UNABLE TO CALCULATE RESULT, REACTION CHECK FAILURE" FOR QUALITY CONTROL AND PATIENT SAMPLES. THE LETTER INSTRUCTS THE CUSTOMER TO DISCONTINUE USE OF THE SUSPECT LOTS AND DESTROY ANY REMAINING INVENTORY. THE CAUSE OF THE STABILITY FAILURE HAS BEEN TRACED TO A CONTAMINATION OF THE BULK MATERIAL.
THE CUSTOMER OBSERVED ERROR CODE 1054 UNABLE TO CALCULATE RESULT, REACTION CHECK FAILURE ON QUALITY CONTROL (QC) WHEN USING THE CK ASSAY (LIST NUMBER 7D63, LOT NUMBER 87697UN18). NO IMPACT TO PATIENT MANAGEMENT WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 551319 | ARCHITECT CREATINE KINASE | CREATINE KINASE (CK) | CGS | ABBOTT MANUFACTURING INC | 87697UN18 | 00380740012878 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | ARCHITECT C8000| ARCHITECT C8000| LN 01G06 SN (B)(4)| LN 01G06 SN (B)(4) |