Biomet 3i, LLC recalls 3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.
- Recall date
- August 8, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2845-2016
- FDA classification
- Class II
- Brand / firm
- Biomet 3i, LLC
- Sold / distributed
- US Distributions to the states of : CA and FL., and Worldwide to : Colombia, France, Germany, Italy, and Spain.
Why it was recalled
Product was incorrectly packaged.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.
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