The Recall Desk
ModerateFDA (Devices)·Z-2022-2017·Announced 2017-05-10

Anspach Effort Recalls 14cm QD Angle Attachment for Pneumatic Systems

The Anspach Effort, Inc. is recalling 238 units of the 14cm QD Angle Attachment 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 involves a documentation issue (missing service interval) rather than a direct physical defect or reported injury, fitting the criteria for a moderate severity recall.

Plain-English summary

The Anspach Effort, Inc. is recalling 238 units of the 14cm QD Angle Attachment, a component 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. QD14 and DFU 18-0048. The recall includes all serial numbers shipped to customers prior to September 27, 2016. The products were distributed worldwide, including nationwide in the United States (specifically HI and DC), Puerto Rico, Guam, and Japan.

Consumers should stop using the affected product and contact The Anspach Effort, Inc. for further instructions on how to proceed with the recall.

The recalled product

Product
14cm QD Angle Attachment Product Usage: Pneumatic system
Affected units
238

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 18-0048
  • Part No. QD14.

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 →