Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122073 |
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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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ELI, Burdick and McKesson brand 280 Resting Electrocardiographs (ELI 280, MLBUR280 and BUR280), Mode... | 2 | 10/02/2021 | Welch Allyn Inc Mortara |
ELI 280 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of t... | 2 | 04/22/2021 | Welch Allyn Inc Mortara |
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