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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K925442
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Product Description
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Recall
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FDA Recall
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Sarns brand Retrograde Cardioplegia Cannulae, manual-inflate, 13 Fr, steerable stylet, ribbed balloo... 2 08/17/2004 Terumo Cardiovascular Systems Corp
Sarns brand Retrograde Cardioplegia Cannulae, manual-inflate, 13 Fr, malleable stylet, ribbed balloo... 2 08/17/2004 Terumo Cardiovascular Systems Corp
Sarns brand Retrograde Cardioplegia Cannulae, manual-inflate, 13 Fr, guidewire stylet, ribbed balloo... 2 08/17/2004 Terumo Cardiovascular Systems Corp
Sarns brand Retrograde Cardioplegia Cannula, 13 Fr, malleable stylet, ribbed balloon, manual-inflate... 2 08/29/2003 Terumo Cardiovascular Systems Corp
Sarns brand Retrograde Cardioplegia Cannula, 13 Fr, steerable stylet, ribbed balloon, manual-inflate... 2 08/29/2003 Terumo Cardiovascular Systems Corp
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