Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Reported: March 21, 2018 Initiated: October 3, 2017 #Z-1011-2018
Product Description
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Reason for Recall
The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.
Details
- Recalling Firm
- Zimmer Biomet, Inc.
- Units Affected
- 8
- Distribution
- US Distribution to states of: FL, WI, MD, MO, and MI.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty. Recalled by Zimmer Biomet, Inc.. Units affected: 8.
Why was this product recalled? ▼
The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 21, 2018. Severity: Moderate. Recall number: Z-1011-2018.
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