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InflammaDry
QUIDEL CORPORATION · Model RPS-ID-20 · UDI-DI 30014613336747
1
510(k) clearances
3
Adverse events
3
Recalls
6
Facilities
Description
InflammaDry
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-03-05 | Quidel Corporation | There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test r |
| 2024-03-05 | Quidel Corporation | There are two windows on the test device, the control line window and the test results window. The line for the test results window were misaligned. In instances of positive test r |
| 2017-06-22 | Quidel Corporation | In-house testing revealed the presence of plastic spurs at the tips of some Sample Collectors. |
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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.