Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101680 |
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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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ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34X... | 2 | 05/21/2021 | Welch Allyn Inc |
Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following mo... | 2 | 04/10/2024 | Baxter Healthcare Corporation |
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