Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K993787 |
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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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Bravo Wellness Kit, Product A1778, each kit packed in a bag or envelope. Each kit contains 1 Triad... | 2 | 01/11/2012 | Heritage Labs International LLC |
Biometric Combo Test Kit, Product K8500, each kit packed in a bag or envelope and contains 1 Triad... | 2 | 01/11/2012 | Heritage Labs International LLC |
AGLH - Lung Health Study, Specimen Collection & Return Kit, Phlebotomy & Urine Kit, Product A2351, 1... | 2 | 01/11/2012 | Heritage Labs International LLC |
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