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SPOTCHEM™ II Uric Acid
ARKRAY USA, INC. · Model 77102 · UDI-DI 00015482771027
10
510(k) clearances
1,513
Adverse events
10
Recalls
26
Facilities
Description
Strip description for the invitro quantitative determination of uric acid concentration in human plasma from whole blood samples
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2022-03-25 | Randox Laboratories Ltd. | Randox have realigned CK-MB Calibrator, CK2393, lot number 4410CK. Calibrating with the new value will cause a positive shift of approximately 6% with both Quality Controls and Pat |
| 2019-05-03 | Siemens Healthcare Diagnostics, Inc. | A steady upward trend in blank (u) absorbance was observed |
| 2019-05-03 | Siemens Healthcare Diagnostics, Inc. | A steady upward trend in blank (u) absorbance was observed |
| 2018-07-18 | Abbott Laboratories, Inc | The product has a stability issue which may lead to an error code indicating "Unable to calculate result, reaction check failure" and/or Quality Control results out of range low. |
| 2018-07-18 | Abbott Laboratories, Inc | The product has a stability issue which may lead to an error code indicating "Unable to calculate result, reaction check failure" and/or Quality Control results out of range low. |
| 2017-06-29 | Siemens Healthcare Diagnostics, Inc. | Various assays used to measure different chemical levels in blood, urine, or cerebrospinal fluid may interfere with the drugs sulfasalazine and/or sulfapyridine causing falsely ele |
| 2017-06-29 | Siemens Healthcare Diagnostics, Inc. | Various assays used to measure different chemical levels in blood, urine, or cerebrospinal fluid may interfere with the drugs sulfasalazine and/or sulfapyridine causing falsely ele |
| 2011-10-19 | Medtest Holdings, Inc. | Linear performance information in product insert does not match that listed in the approved premarket notification |
| 2007-10-12 | Abbott Laboratories Inc. | Three potential issues with Creatine Kinase Lot Number: 52044HW00: (1) Decrease in quality control and/or patient results (2) An iIncreased imprecision, or (3) Error Code 1054 (U |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.