Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K132066 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests | 2 | 04/24/2024 | Quidel Corporation |
| QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests | 2 | 04/24/2024 | Quidel Corporation |
| InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay... | 2 | 08/01/2017 | Quidel Corporation |
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