Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K141557 |
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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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Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715 | 2 | 10/19/2021 | ADRIA SRL |
Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749 | 2 | 10/19/2021 | ADRIA SRL |
Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745 | 2 | 10/19/2021 | ADRIA SRL |
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