Medical Device Recalls
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21 to 24 of 24 Results
510(K) Number: K063618 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Terumo TenderFlow Pediatric Arterial Cannulae, 5.3 mm (16 Fr) OD, with 1/4 inch vented connector, 9... | 2 | 07/10/2007 |
FEI # 1828100 Terumo Cardiovascular Systems Corp |
| Terumo TenderFlow Pediatric Arterial Cannulae, 5.3 mm (16 Fr) OD, with 1/4 inch vented connector, 9 ... | 2 | 02/06/2009 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo TenderFlow Pediatric Arterial Cannulae, 5.3mm (16 Fr) OD, with 1/4 inch non-vented connector... | 2 | 07/10/2007 |
FEI # 1828100 Terumo Cardiovascular Systems Corp |
| Terumo TenderFlow Pediatric Arterial Cannulae, 5.3mm (16 Fr) OD, with 1/4 inch non-vented connector,... | 2 | 02/06/2009 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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