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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Recalling Firm
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Z-0546-05 - Sodium Chloride Injection USP, manufactured by IV Flush LLC 1 03/01/2005 FEI # 3004978897
IV Flush LLC
Z-0545-05 - Heparin Lock Flush Solution, manufactured by IV Flush LLC 1 03/01/2005 FEI # 3004978897
IV Flush LLC
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