Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173765 |
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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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Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted softwar... | 2 | 04/22/2021 | Welch Allyn Inc Mortara |
Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor under the following device names:... | 2 | 04/29/2020 | WELCH ALLYN, INC/MORTARA |
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