Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K962581 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Baxter Interlink System Buretrol Solution Set with Large Bore 4-Way Stopcock with Rotating Male Luer... | 2 | 03/24/2006 | Baxter Healthcare Corp. |
| Baxter Interlink System Buretrol Solution Set with Large Bore 4-Way Stopcock Extension Set and Miniv... | 2 | 03/24/2006 | Baxter Healthcare Corp. |
| Baxter Interlink System Buretrol Solution Set with Large Bore 3-Way Stopcock with Rotating Male Luer... | 2 | 03/24/2006 | Baxter Healthcare Corp. |
| Baxter ClearLink Intravenous (IV) Solution Sets and Extension Sets that have a ClearLink luer activ... | 2 | 05/17/2005 | Baxter Healthcare Corp. |
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