Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K072105 |
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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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BD Alaris PCU REF 8015 | 1 | 11/07/2023 | CareFusion 303, Inc. |
Alaris PCA Module 8120 | 1 | 11/07/2023 | CareFusion 303, Inc. |
BD Alaris Syringe Module, REF 8110 | 1 | 11/07/2023 | CareFusion 303, Inc. |
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses f... | 2 | 03/01/2023 | CareFusion 303, Inc. |
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