Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K010582 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020 | 2 | 08/18/2025 |
FEI # 3004386693 Mckesson Medical-Surgical Inc. Corporate Office |
| Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008 | 2 | 09/19/2024 |
FEI # 1451040 Cypress Medical Products LLC |
| Strep test: a. McKesson Medical-Surgical McKesson Rapid Test Kit McKesson Consult Infectious Disea... | 2 | 08/26/2022 |
FEI # 3004386693 Mckesson Medical-Surgical Inc. Corporate Office |
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