Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K191599 |
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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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| NICO Myriad-LX Illumination Pack: REF: NN-1000 Mvriad-LX Illumination Pack. 11ga REF: NN-1001 Mvri... | 2 | 06/09/2021 |
FEI # 3007456622 Nico Corp. |
| NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN... | 2 | 11/26/2025 |
FEI # 3015967359 Stryker Corporation |
| NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; ... | 2 | 11/26/2025 |
FEI # 3015967359 Stryker Corporation |
| NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-... | 2 | 11/26/2025 |
FEI # 3015967359 Stryker Corporation |
| Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissu... | 2 | 06/09/2021 |
FEI # 3007456622 Nico Corp. |
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