Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K163646 |
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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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| Terragene Bionova PCD (PCD222-C) | 2 | 01/26/2024 | TERRAGENE S.A. |
| ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device, REF 73135. | 2 | 02/27/2025 | TERRAGENE S.A. |
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