Navilyst Medical recalls

Navilyst Medical has 73 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 4 Mar 2015. The most frequent reason is sterility.

Total recalls73since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 4 Mar 2015

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 73 100%Class III 0 0%

Why navilyst medical is recalled

By year

All navilyst medical recalls, newest first

73 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IINamic Convenience Kit, Radiology Kit, Upn H749601014911 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749601113111 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Cath Kit, Upn H7496010018151 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H9656002072121 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H965601206511 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, 3 Valve Manifold Kit, Upn H749600411611 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H7496005001131 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749601900431 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H749601907851 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Hopkins Left Heart, Upn H749601836621 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749600309351 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H965600416321 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Dye Cath Lab Kit, Upn H749601367131 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H7496001001111 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H965PK193168S1 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749602000571 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H965601017731 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H749601314811 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H749601801561 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H749601399921 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Neuro Angio Kit, Upn H749600202361 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H965600338021 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H965600125911 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, 3V Manifold Kit, Upn H965601011621 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Angio Kit, Upn H749601319961 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, UPN H749600329421 recalled by Navilyst MedicalNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749601605351 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749600618011 recalledNavilyst MedicalSterilityNationwide
DeviceCLASS IINamic Convenience Kit, Left Heart Kit, Upn H749601506721 recalledNavilyst MedicalSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.