Dimension Vista Enzymatic Creatinine (ECREA) reagent, SMN 10700444
FDA device recall Z-1233-2020 · posted 2020-01-24 · Terminated
Recall details
- Recalling firm
- Siemens Healthcare Diagnostics, Inc.
- Reason for recall
- There is a potential for falsely depressed creatinine results for patients on phenindione therapy when using the enzymatic methodology. Interference has not been observed with the creatinine Jaffe methodology.
- Action taken
- Siemens Healthcare Diagnostics initiated a customer communication for this issue via letter beginning December 18, 2019.
- Root cause
- Under Investigation by firm
- Status
- Terminated
- Product code
- JFY
- Quantity affected
- 11,725 units
- Distribution
- US Nationwide
- Date initiated
- 2019-12-18
- Date posted
- 2020-01-24
- Date terminated
- 2020-06-25
- Location
- Tarrytown, NY
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| DIMENSION VISTA ENZYMATIC CREATININE FLEX REAGENT CARTRIDGE, AND ENZYMATIC CREATININE CALIBRATOR, MODELS K1270, KC270 (K090330) | Siemens Healthcare Diagnostics, Inc. | 2009-05-22 |