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Immunalysis
IMMUNALYSIS CORP · Model 305UR-0060W · UDI-DI 00840937101254
LDJ
Prescription
1
510(k) clearances
2
Adverse events
15
Recalls
101
Facilities
Description
Cannabinoids Urine HEIA™
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-04 | Family Dollar Stores, Llc. | Products were stored outside of labeled temperature requirements. |
| 2022-06-23 | Family Dollar Stores, Llc. | Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022. |
| 2020-08-18 | Ameditech Inc | Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. |
| 2020-08-18 | Ameditech Inc | Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. |
| 2020-08-18 | Ameditech Inc | Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. |
| 2020-08-18 | Ameditech Inc | Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. |
| 2020-08-18 | Ameditech Inc | XXX |
| 2020-08-18 | Ameditech Inc | Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. |
| 2020-08-18 | Ameditech Inc | Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. |
| 2020-02-10 | Carolina Liquid Chemistries Corp | Corrections are being made to the device labeling regarding its intended use, to include a statement clarifying it is for research purposes only. |
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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.
