Anspach Electronic Foot Control Recalled for Missing Service Interval
The Anspach Effort, Inc. is recalling 209 Electronic Foot Controls with Direction Switches because the supplied directions for use did not contain a recommended service interval.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text identifies the issue as a missing service interval in the documentation without reporting any injuries, illnesses, or specific safety hazards, fitting the criteria for a moderate severity labeling/documentation issue.
Plain-English summary
The Anspach Effort, Inc. is recalling 209 units of the Electronic Foot Control with Direction Switch (Part No. E-FP-DIR). The recall is being conducted because the supplied Directions for Use (DFU) did not contain a recommended service interval.
The affected products were distributed worldwide, including US Nationwide in the states of HI, DC, Puerto Rico, and the countries of Guam and Japan. The recall covers all product shipped prior to 09/27/2016, identified by DFU 18-0085.
Consumers should contact The Anspach Effort, Inc. for further instructions regarding the missing service interval information.
The recalled product
- Product
- Electronic Foot Control with Direction Switch Product Usage: Electric system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 209
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All product shipped prior to 09/27/2016
- DFU 18-0085
- Part No. E-FP-DIR.
Distribution
Part of a larger recall action
This product is one of 103 recalled by The Anspach Effort, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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