Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K992231 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Fountain Infusion System, 4F, REF IS4-90-50, Sterile, Merit Medical Systems, Inc., South Jordan, Uta... | 2 | 09/11/2008 | Merit Medical Systems, Inc. |
| Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY | 2 | 01/02/2024 | Merit Medical Systems, Inc. |
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