Medical Device Recalls
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1 result found
510(K) Number: K012455 |
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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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| Welch Allyn DuraShock Aneroid Gauge Sets with a Reusable Blood Pressure Cuff labeled as: 1) WELCH... | 2 | 04/15/2025 | Baxter Healthcare Corporation |
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