Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K992723 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT orthopedic perioper... | 2 | 08/30/2018 | Haemonetics Corporation |
Haemonetics OrthoPAT -Orthopedic Perioperative Autotransfusion System US Only: 1050-110-ENG Outsid... | 2 | 06/07/2011 | Haemonetics Corporation |
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