Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K090547 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular, Inc.), UltraClip® Dual Trigger Bre... | 2 | 06/10/2013 | Bard Peripheral Vascular Inc |
USHER® Support Catheter- Angled Tip WL130cm, RI 7F; REF USH07AT; PK1022-01A; Rx only, Non-Pyrogenic... | 2 | 06/10/2013 | Bard Peripheral Vascular Inc |
MICROSHEATH® - 0.066 (1.7mm) proximal, 0.064 (1.6mm); WL 123cm, RGC 8F Guide; minimum ID: 0.086"/ (2... | 2 | 06/10/2013 | Bard Peripheral Vascular Inc |
BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular, Inc.), UltraClip® Dual Trigger Bre... | 2 | 06/10/2013 | Bard Peripheral Vascular Inc |
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