Class II — The Anspach Effort, Inc.
| Recalling firm | THE ANSPACH EFFORT, 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 | Has the incorrect operating directions on the mode switch ring, i.e. its is labeled "FWD, LOCK, REV" instead of "ON, LOCK, ON". |
| Product | Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc. |
| Quantity | 20 hand pieces |
| Distribution | US Distribution to the state of : VA and Internationally to: Thailand and UK |
| Initiated | 2015-11-25 |
| Classified | 2016-07-05 |
| Terminated | 2018-11-14 |
| Recall number | Z-2126-2016 |
| 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 — The Anspach Effort, Inc. (Z-2126-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73198/
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