Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K993203 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine ... | 2 | 08/26/2022 | Mckesson Medical-Surgical Inc. Corporate Office |
ICON DS hCG, an in-vitro diagnostic. Part number 44025. | 2 | 04/02/2003 | Beckman Coulter Inc |
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