List view Cards view
Name Date Date initiated Country Source
Recall of Device Recall ARCHITECT Estradiol Reagent 2007-02-19 United States USFDA
Recall of Device Recall CELLDYN 4000 2004-05-12 United States USFDA
Recall of Device Recall iSite PACS 2007-02-14 United States USFDA
Recall of Device Recall MicroMaxx LAP Transducer 2007-02-05 United States USFDA
Recall of Device Recall EpiFix 2007-02-15 United States USFDA
Recall of Device Recall CIC Pro System 2007-01-24 United States USFDA
Recall of Device Recall BioRad TOX/See 2007-02-12 United States USFDA
Recall of Device Recall Precision Spinal Cord Stimulation System 2007-01-30 United States USFDA
Recall of Device Recall Thyrotest TSH POC Rapid membrane test 2007-01-24 United States USFDA
Recall of Device Recall HeartStart FR2 2007-02-28 United States USFDA
Recall of Device Recall CADD Prizm 2007-01-19 United States USFDA
Recall of Device Recall LIFEPAK 2007-03-02 United States USFDA
Recall of Device Recall Steris QFC1728 and QFC1729 Quick Connects 2007-02-23 United States USFDA
Recall of Device Recall PADPRO DULT Radiotranslucent Pad w/Zoll connector 2007-03-08 United States USFDA
Recall of Device Recall PADPRO ADULT Radiotranslucent Pad w/Medtronic connector 2007-03-08 United States USFDA
Recall of Device Recall OEC 9900 Elite 2007-03-01 United States USFDA
Recall of Device Recall OEC 9800 2007-03-01 United States USFDA
Recall of Device Recall OEC 8800 2007-03-01 United States USFDA
Recall of Device Recall DeVilbiss 535DX CF Continuous Flow Cylinder (Oxygen) 2007-01-24 United States USFDA
Recall of Device Recall Bausch & Lomb ReNu MultiPurpose Solution, Equate MultiPurpose Solution and Target Brand MultiPur 2007-03-05 United States USFDA
Recall of Device Recall Ceegraph/Sleepscan Netlink Traveler 2007-02-26 United States USFDA
Recall of Device Recall SafeClinitubes, REF 942892. 2006-06-22 United States USFDA
Recall of Device Recall Brilliance CT 2006-11-06 United States USFDA
Recall of Device Recall VITROS Immunodiagnostics Products HBsAg Reagent Pack 2007-02-01 United States USFDA
Recall of Device Recall Qualicheck 1, Aqueous Quality Control, Level 2, S7140, REF 944042. 2006-06-06 United States USFDA