Medical Device Recalls
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1 result found
510(K) Number: K122262 |
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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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Haemonetics® OrthoPAT® System-OPAT QuickConnect Reservoirs. Product Code: OPT-R-1000 The OrthoPA... | 2 | 08/30/2018 | Haemonetics Corporation |
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