Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
Reported: November 28, 2018 Initiated: October 22, 2018 #Z-0496-2019
Product Description
Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
Reason for Recall
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
Details
- Recalling Firm
- Zimmer Biomet, Inc.
- Units Affected
- 8 units
- Distribution
- AR, MO, MN, NJ, NY, OH, MN , NJ, VA
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108. Recalled by Zimmer Biomet, Inc.. Units affected: 8 units.
Why was this product recalled? ▼
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 28, 2018. Severity: Moderate. Recall number: Z-0496-2019.
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