Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K020753 |
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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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DeRoyal (R) Umbilicup, REF 72-8000NS, Rx Only, Manufactured by DeRoyal, Powell, TN 37849 Produc... | 2 | 04/12/2012 | DeRoyal Industries Inc |
DeRoyal (R) Umbilicup, REF 72-8000, Rx Only, STERILE EO, Manufactured by DeRoyal, Powell, TN 37849 ... | 2 | 04/12/2012 | DeRoyal Industries Inc |
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