Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K820297 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Custom Cardiovascular Procedure Kits; Over-Pressure Safety Valves. For use only in the extracorpo... | 2 | 06/23/2015 | Terumo Cardiovascular Systems Corp |
Custom surgical kits containing TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 and (b) LH130J ... | 2 | 06/21/2018 | Terumo Cardiovascular Systems Corporation |
TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 (b) LH130J | 2 | 06/21/2018 | Terumo Cardiovascular Systems Corporation |
Terumo Cardiovascular Custom Cardiovascular Procedure Kits containing an Overpressure Safety Valve, ... | 2 | 12/27/2013 | Terumo Cardiovascular Systems Corporation |
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