Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K932740 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
-