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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 07/30/2014
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Product Description
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FDA Recall
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Z-2415-2011 - Pinnacle Destination Guiding Sheath, 6 French, 90 cm, Straight Tip, Tuohy-Borst Valve, Lot MD24, MD31, ME07, & ME14. 510(k) K012812 Guiding Sheath is used to facilitate the introduction of interv... 2 06/06/2011 Terumo Medical Corporation
Z-2417-2011 - Pinnacle Destination Guiding Sheath, 6 French, 45 cm, Hockey Stick Tip, Tuohy-Borst Valve, Lot ME07, 510 (K) K012854 Guiding Sheath is used to facilitate the introduction of interventional and diag... 2 06/06/2011 Terumo Medical Corporation
Z-2416-2011 - Pinnacle Destination Guiding Sheath, 7 French, 90 cm, Straight Tip, Tuohy-Borst Valve, Lots ME07 & MF12, 510(k) K052185 Guiding Sheath is used to facilitate the introduction of interventional and d... 2 06/06/2011 Terumo Medical Corporation
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