Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K983162 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Baxter Peri-Guard Repair Patch (legacy product codes): a) PC0404NBIO, b) PC0608NBIO, c) PC0814... | 2 | 03/26/2024 | Baxter Healthcare Corporation |
| Baxter Supple Peri-Guard Repair Patch (legacy product codes): a) PC0404SNBIO, b) PC0608NSBIO, ... | 2 | 03/26/2024 | Baxter Healthcare Corporation |
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