Home / Brands / Insight Instruments
Insight Instruments Recalls
3 recalls on record · May 22, 2013 to February 12, 2014 · Drugs, Medical Devices
Recalls by year
13
14
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 12, 2014DrugsFDA
Insight Instruments, Inc. recalls Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe, Rx Only. Manufactured by: Insight Instruments, Inc., 2580 SE
Hazard: Marketed without an Approved NDA/ANDA.
November 13, 2013Medical DevicesFDA
Insight Instruments, Inc. recalls MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25- gauge illuminator for vitreo-retinal surge
Hazard: The product was registered and distributed as a Class I medical device and was subsequently determined to be a Class II medical device which requires FDA market clearance.
May 22, 2013Medical DevicesFDA
Insight Instruments, Inc. recalls Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot tubes work like a ceiling light while s
Hazard: Insight Instruments, Inc., Stuart, FL is recalling M.I.S. (Multi-Port Illumination System), Ophthalmic Cannula due to a misclassification of the medical device.