PlainRecalls
FDA Devices Moderate Class II Terminated

ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001

Reported: October 13, 2021 Initiated: September 9, 2021 #Z-0074-2022

Product Description

ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001

Reason for Recall

Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery

Details

Recalling Firm
DePuy Orthopaedics, Inc.
Units Affected
10 units
Distribution
US Nationwide distribution in the states of CA, LA, MN, MO, NC, NE, OR, PA, WA, WI.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001. Recalled by DePuy Orthopaedics, Inc.. Units affected: 10 units.
Why was this product recalled?
Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery
Which agency issued this recall?
This recall was issued by the FDA Devices on October 13, 2021. Severity: Moderate. Recall number: Z-0074-2022.