Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K011097 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp. | 2 | 05/12/2026 |
FEI # 2024674 Quidel Corporation |
| QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC | 2 | 09/10/2025 |
FEI # 2024674 Quidel Corporation |
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