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 | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| Product | Bearing Sleeve, 15CM Straight Product Usage: Pneumatic system |
| Quantity | 568 |
| Distribution | Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan |
| Initiated | 2016-10-06 |
| Classified | 2017-05-04 |
| Terminated | 2019-07-26 |
| Recall number | Z-2006-2017 |
| 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-2006-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76059/
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