Medical Device Recalls
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11 to 11 of 11 Results
Recall Date to: 03/01/2015 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 with Sterile Fluid Path Package Model Number: 4050-170N | 2 | 02/15/2007 | Atrium Medical Corporation |
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