Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 07/25/2014 510(K) Number: K043140 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusio... | 2 | 07/01/2014 | Atrium Medical Corporation |
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