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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K932740
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Product Description
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FDA Recall
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ON-Q PainBuster with OnDemand (270 ml, 2 ml/hr + 5 ml bolus /60 min refill), Model PMB01, I-Flow Cor... 2 10/06/2007 I-Flow Corporation
I-Flow ON-Q PainBuster (100 ml, 2 mI/hr) Pump, PM012, Lot #662449 and 662742 2 01/18/2007 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
Homepump Eclipse Infusion Pump, Disposable Elastomeric Infusion System (100 ml x 50 ml/hr) Model E1... 2 03/27/2003 I-Flow Corporation
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