Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K001368 |
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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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PhaSeal Injector Luer Lock, Item No. 31, US Order No. 10310 | 2 | 08/22/2007 | Carmel Pharma, Inc. |
PhaSeal, Protector 14, Item No. P14, US Order No. 21320 | 2 | 08/22/2007 | Carmel Pharma, Inc. |
PhaSeal, Protector 21, Item No. 21, US Order No. 22020 | 2 | 08/22/2007 | Carmel Pharma, Inc. |
PhaSeal, Protector 50, Item No. 50, US Order No. 10310 | 2 | 08/22/2007 | Carmel Pharma, Inc. |
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