Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K993387 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Baxter I-Pump Pain Management System infusion pump, product codes 2L3107, 2L3107K and 2L3107R, Baxte... | 2 | 04/26/2006 | Baxter Healthcare Corp. |
| Baxter I-Pump Pain Management System infusion pump, product codes 2L3107, 2L3107K and 2L3107R, Baxte... | 2 | 04/26/2006 | Baxter Healthcare Corp. |
| Baxter I-Pump Pain Management System infusion pump, product codes 2L3107, 2L3107K and 2L3107R, Baxte... | 2 | 11/16/2005 | Baxter Healthcare Corp. |
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