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Biomet, Inc. recalls A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
Recalled July 22, 2015 · FDA recall Z-2072-2015 · Biomet
Hazard
Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone. · FDA Class II
Units
223
Sold at
Domestic: TX NJ, NC, KY, MA, SD, MO, AL, IN, GA, AR International: Netherlands, Japan, Costa Rica
Description
Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone.
Product
A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →