Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 04/02/2015 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1611-2013 - Pinnacle® Destination® Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the h... | 2 | 06/27/2013 | Terumo Medical Corporation |
Z-1612-2013 - Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or artery. | 2 | 06/27/2013 | Terumo Medical Corporation |
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