Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K090882 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Merit Medical's Custom Procedural Tray or Kits K12T-03162B & K12T-02641F.Custom Procedural ... | 2 | 01/10/2013 |
FEI # 3002975287 Merit Medical Systems, Inc. |
| 0.9% Sodium Chloride Injection, USP, pre-filled flush solution, for IV Flush only, sterile fluid pat... | 2 | 01/11/2012 |
FEI # 3013319212 Hospira Inc. |
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