Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K120630 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF number... | 2 | 02/13/2020 | Microvention, Inc. |
| Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers 45-681026, 45-681434, 4... | 2 | 02/13/2020 | Microvention, Inc. |
| Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers 45-781032, 45-781238, 45-... | 2 | 02/13/2020 | Microvention, Inc. |
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