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.
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