Medical Device Recalls
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1 result found
510(K) Number: K151762 |
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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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Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only | 2 | 02/17/2022 | Merete Medical GmbH |
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