"***Electric Systems Foot Control with Direction Only***Rx Only***"… — Class II medical device recall Z-0075-2013
Terminated recall by The Anspach Effort, Inc., reported 2012-10-24, distributed nationwide. The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Co
| Recall number | Z-0075-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2012-01-09 |
| Classified | 2012-10-17 |
| Reported by FDA | 2012-10-24 |
| Terminated | 2014-09-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | CH, IT, JP, TR, TW |
| Quantity | 41 units |
| Serial numbers | E2830521009, E2830527100, E28305271001, E28305271002, E28305271003, E28305271004, E28305271006, E28305271007, E28305271008, E28305271010, E29, E29305270901, E29305270902, E29305270903, E29305271101, E29305271102, E29305271103, E29305271104, E29305271105, E29305271106, E29305271107 |
Product
"***Electric Systems Foot Control with Direction Only***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
Reason for recall
The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0075-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.