Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K073050 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PowerLoc MAX Safety Winged Infusion Set, Product Code 0132215 The PowerLoc MAX Safety Winged Infu... | 2 | 04/30/2015 | Bard Access Systems |
| BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: SafeStep Port Access ... | 2 | 03/13/2015 | Bard Access Systems |
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