Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K192247 |
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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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The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 ... | 2 | 12/01/2021 | Magnolia Medical Technologies, Inc. |
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be u... | 2 | 08/31/2021 | Magnolia Medical Technologies, Inc. |
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