Class II — Ebi, Llc
| Recalling firm | EBI, LLC - AHP EOS Buyer Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Broken screw insertor hardness was measured and found to be below the acceptable limits. |
| Product | Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178 |
| Quantity | 15 units |
| Distribution | Nationwide Distribution, including the states of MO, TX, and IN. |
| Initiated | 2012-09-29 |
| Classified | 2012-12-17 |
| Terminated | 2015-12-07 |
| Recall number | Z-0536-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Ebi, Llc (Z-0536-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/63653/
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