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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K090882
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FDA Recall
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Merit Medical's Custom Procedural Tray or Kits K12T-03162B & K12T-02641F.Custom Procedural ... 2 01/10/2013 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 Hospira Inc.
Excelsior Disposable Syringe W/Normal Saline (0.9% sodium Chloride) General hospital use 1 10/20/2010 Excelsior Medical Corp