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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K052117
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FDA Recall
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I-Flow Corporation Easy Pump LT 60-24 (60 ml x 2 ml/hr), REF: 04434366, assembled in Mexico. The... 2 09/14/2009 I-Flow Corporation
Easypump ST 100-1 infusion pump 2 03/07/2006 I-Flow Corporation
Easypump L T 60-24 infusion pump 2 03/07/2006 I-Flow Corporation
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