Anspach Effort Bearing Sleeve Recall for Missing Service Interval
The Anspach Effort, Inc. is recalling 58 Bearing Sleeve units because the supplied directions for use did not contain a recommended service interval.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 a documentation issue (missing service interval) without reporting any injuries, illnesses, or specific mechanical failures, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
The Anspach Effort, Inc. is recalling 58 units of the Bearing Sleeve, 19CM Straight Taper, which is used in pneumatic systems. The recall was initiated because the supplied Directions for Use (DFU) did not contain a recommended service interval.
The affected units are identified by Part No. MA-19ST and DFU 18-0099. The recall includes all serial numbers shipped to customers prior to 09/27/2016. The products were distributed worldwide, including US Nationwide in the states of HI, DC, Puerto Rico, Guam, and Japan.
Consumers should stop using the affected Bearing Sleeve units and contact The Anspach Effort, Inc. for further instructions.
The recalled product
- Product
- Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 58
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-19ST.
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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