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 | The Cypher MIS Screw Inserter may exhibit an increased rate of instrument tip failure. |
| Product | Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal Screw Fixation System. |
| Quantity | 32 units (30 domestic and 2 international) |
| Distribution | Worldwide Distribution - USA (nationwide) and the country The Netherlands. |
| Initiated | 2014-05-15 |
| Classified | 2014-06-17 |
| Terminated | 2017-04-21 |
| Recall number | Z-1811-2014 |
| 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-1811-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68526/
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