Medical Device Recalls
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1 result found
510(K) Number: K122473 |
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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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HILLROM PROGRESSA+ BED, Product Codes: P7501A000016, P7501A000019, P7501A000031, P7501A000032, P750... | 2 | 11/02/2023 | Baxter Healthcare Corporation |
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