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Stradis Healthcare, LLC. recalls Eye Pack - contains Devon Light Glove Used during surgery
Recalled July 15, 2015 · FDA recall Z-2023-2015 · Stradis Healthcare
Hazard
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits. · FDA Class II
Units
One
Sold at
Distribution US nationwide to AL, AK, CA, DE, FL, GA, HI, ID, IL, IN, KS, KY, ME, MD, MA, MI, MS, MO, NM, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA; Canada and Dubai
Description
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Product
Eye Pack - contains Devon Light Glove Used during surgery
Manufacturer(s)
Stradis Healthcare, LLC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →