3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.
Reported: September 28, 2016 Initiated: August 8, 2016 #Z-2845-2016
Product Description
3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.
Reason for Recall
Product was incorrectly packaged.
Details
- Recalling Firm
- Biomet 3i, LLC
- Units Affected
- 92 units
- Distribution
- US Distributions to the states of : CA and FL., and Worldwide to : Colombia, France, Germany, Italy, and Spain.
- Location
- Palm Beach Gardens, FL
Frequently Asked Questions
What product was recalled? ▼
3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.. Recalled by Biomet 3i, LLC. Units affected: 92 units.
Why was this product recalled? ▼
Product was incorrectly packaged.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 28, 2016. Severity: Moderate. Recall number: Z-2845-2016.
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