Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K203060 |
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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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VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF) | 2 | 07/28/2023 | Johnson & Johnson Surgical Vision, Inc. |
Veritas Advanced Infusion Packs, REF: VRT-AI | 2 | 01/20/2023 | Johnson & Johnson Surgical Vision, Inc. |
Veritas Advanced Infusion Packs. Used in ophthalmic procedures. | 2 | 10/12/2022 | Johnson & Johnson Surgical Vision, Inc. |
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