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AcuFocus Recalls

1 recall on record · March 30, 2016 to March 30, 2016 · Medical Devices

March 30, 2016Medical DevicesFDA

AcuFocus, Inc. recalls KAMRA Inlay, ACI 7000 Corneal Inlay, Part No. 76195-01 and 76195-10 (OUS) Labeling: The KAMRA inlay is indicated for

Hazard: AcuFocus is recalling KAMRA ACI 7000 Corneal Inlays due to concerns with the labeled shelf life.

AcuFocus Recalls | RecallWatchUSA