Anspach Effort Recalls Autolube-III Pneumatic Systems for Missing Service Interval
The Anspach Effort, Inc. is recalling 17 Autolube-III pneumatic systems because the supplied directions for use did not include 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, and the hazard involves a documentation error (missing service interval) rather than a direct physical defect or reported injury, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
The Anspach Effort, Inc. is recalling 17 units of the Autolube-III with Foot Guard pneumatic system. The recall was initiated because the supplied Directions for Use (DFU) did not contain a recommended service interval.
The affected products were distributed worldwide, including in the United States (specifically HI, DC, and PR) and in the countries of Guam and Japan. The recall covers all product shipped prior to September 27, 2016, identified by DFU 18-0040 and Part No. AUTOLUBE-III-FG.
Consumers who possess this product should contact The Anspach Effort, Inc. for further instructions regarding the missing service interval information.
The recalled product
- Product
- Autolube-III with Foot Guard Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Affected units
- 17
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 18-0040
- Part No. AUTOLUBE-III-FG
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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