Anspach Effort Recalls Bearing Sleeves Due to Missing Service Interval
The Anspach Effort, Inc. is recalling 182 Bearing Sleeve, 10CM Curved units 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, and the hazard is a documentation issue (missing service interval) without reported injuries or illnesses, fitting the criteria for a moderate severity recall.
Plain-English summary
The Anspach Effort, Inc. is recalling 182 units of the Bearing Sleeve, 10CM Curved, which is used in pneumatic systems. The recall is being conducted because the supplied directions for use (DFU) did not contain a recommended service interval.
The affected products are identified by Part No. MA-10C and DFU 18-0099. The recall includes all serial numbers shipped to customers prior to 09/27/2016. These products were distributed worldwide, including US Nationwide in the states of HI, DC, Puerto Rico, Guam, and Japan.
Consumers should stop using the affected products and contact The Anspach Effort, Inc. for further instructions.
The recalled product
- Product
- Bearing Sleeve, 10CM Curved Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 182
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 serial numbers shipped to customers prior to 09/27/2016
- DFU 18-0099
- Part No. MA-10C.
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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