Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K063740 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Systems (Part Number M8275093/5). ... | 2 | 05/30/2017 | KCI USA, INC. |
| AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cor... | 2 | 01/25/2010 | KCI USA, Inc. |
| 500 mL InfoV.A.C. Canisters (with Gel); Part #M8275063/5 (5 canister pack) and Part #M8275063/10 (10... | 2 | 09/20/2008 | KCI USA, Inc. |
| 500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 ... | 2 | 09/20/2008 | KCI USA, Inc. |
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