Medical Device Recalls
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1 result found
510(K) Number: K192358 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily reli... | 2 | 04/18/2023 |
FEI # 3012316249 Compass Health Brands (Corporate Office) |
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