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DePuy Orthopaedics, Inc. recalls ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Recalled October 13, 2021 · FDA recall Z-0074-2022 · DePuy Orthopaedics
Hazard
Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery · FDA Class II
Units
10 units
Sold at
US Nationwide distribution in the states of CA, LA, MN, MO, NC, NE, OR, PA, WA, WI.
Description
Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery
Product
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Manufacturer(s)
DePuy Orthopaedics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →