Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K142105 |
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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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Baxter Electrocardiograph, ELI 380 -DCS21 | 2 | 01/24/2023 | Baxter Healthcare Corporation |
ELI 380 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of t... | 2 | 04/22/2021 | Welch Allyn Inc Mortara |
ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance, multichannel resting ... | 2 | 06/12/2015 | Mortara Instrument, Inc |
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