The Recall Desk
ModerateFDA (Devices)·Z-2007-2017·Announced 2017-05-10

Anspach Effort Bearing Sleeve Recalled for Missing Service Interval Instructions

The Anspach Effort, Inc. is recalling 121 Bearing Sleeves 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) rather than a direct physical defect or reported injury, fitting the Moderate criteria for minor labeling/documentation errors.

Plain-English summary

The Anspach Effort, Inc. is recalling 121 units of the Bearing Sleeve, 15CM 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 products were distributed worldwide, including US Nationwide in the states of HI, DC, Puerto Rico, Guam, and Japan. The recall covers all serial numbers shipped to customers prior to September 27, 2016, identified by DFU 18-0099 and Part No. MA-15ST.

Consumers should stop using the affected bearing sleeves and contact The Anspach Effort, Inc. for further instructions.

The recalled product

Product
Bearing Sleeve, 15CM Straight Taper Product Usage: Pneumatic system
Affected units
121

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-15ST.

Distribution

Distributed nationwide across the United States.

The notice also names 3 states specifically:

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.

See all 103 products in this recall →