American Medical Systems Innovation Center - Silicon Valley recalls

American Medical Systems Innovation Center - Silicon Valley has 32 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 29 Jul 2015. The most frequent reason is sterility.

Total recalls32since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 29 Jul 2015

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 32 100%Class III 0 0%

Why american medical systems innovation center - silicon valley is recalled

By year

All american medical systems innovation center - silicon valley recalls, newest first

32 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIStripper Disposable EndoStat Fiber recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IISureflex 150 Lithotripsy Fiber, 5x, Blue recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IISureflex 365 Lithotripsy Fiber, 5x, Blue recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IISureflex 200 Lithotripsy Fiber, 5x, Blue recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIFiber Stripper, 200¿m, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, StripperW/BLD, 10S, Nonautoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIFiber Stripper, 910¿m, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 28S, Nonautoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIFiber Stripper, 273¿m, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIStripper Disposable EndoStat Fiber recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIStripper Disposable EndoStat Fiber recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 18S, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 12S, Nonautoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IISureflex 550 Lithotripsy Fiber, 5x, Blue recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 14S, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IISureflex 910 Lithotripsy Fiber, 5x, Blue recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IICleaving Tiles recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIFiber Stripper, 365¿m, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS II365¿M Lithotripsy Fiber- Reusable recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IISureflex 273 Lithotripsy Fiber, 5x, Blue recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS II200¿M Lithotripsy Fiber- Reusable recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 14S, Nonautoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 28S, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 44S, Nonautoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 12S, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIFiber Stripper, 550¿m, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, StripperW/BLD, 10S, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIFiber Stripper, 150¿m, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IIStripper Disposable EndoStat Fiber recalled by American Medical SystemsAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide
DeviceCLASS IITool, Stripper W/BLD, 44S, Autoclavable recalledAmerican Medical Systems Innovation Center - Silicon ValleySterilityNationwide

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.