The Recall Desk
ModerateFDA (Devices)·Z-1930-2017·Announced 2017-05-10

Anspach Effort Recalls 14cm QD Angle Attachment for Missing Service Interval

The Anspach Effort, Inc. is recalling 14cm QD Angle Attachments 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, but the source text explicitly states the issue is a missing service interval in the documentation, which aligns with the rubric for minor labeling or documentation issues without reported injuries.

Plain-English summary

The Anspach Effort, Inc. is recalling 14cm QD Angle Attachments. The recall was initiated because the supplied Directions for Use (DFU) did not contain a recommended service interval.

The affected products are identified by Part No. QD14 and DFU 18-0048. The recall includes all serial numbers shipped to customers prior to 09/27/2016. The products were distributed worldwide, including in the United States (specifically HI and DC), Puerto Rico, Guam, and Japan.

Consumers should check their product for the specific part number and serial number date to determine if it is affected. The source text does not provide specific instructions for consumers on how to return the product or what to do if they have already used it.

The recalled product

Product
14cm QD Angle Attachment Product Usage: Product attachment

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 →