Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 01/25/2015 510(K) Number: K930620 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, arterial ... | 3 | 02/27/2007 | Terumo Cardiovascular Systems Corp |
Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, arterial ... | 3 | 02/27/2007 | Terumo Cardiovascular Systems Corp |
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