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  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
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
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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