The Anspach Effort, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1875-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

ANSPACH***Knotless Suture Anchor Deployment Tool, Custom***Rx Only*** This device is intended to be used with Anspach Systems

Product Classification:

Class II

Date Initiated: November 28, 2012

Date Posted: July 2, 2014

Recall Number: Z-1875-2014

Event ID: 64247

Reason for Recall:

The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the Anspach Custom Devices. The units and the records of these products were not consistent with Quality System requirements.

Status: Terminated

Product Quantity: 4

Code Information:

Part Numbers: 98-0006, 98-0009. Serial Numbers: 20030001, 20030002 20033501, 20033502.

Distribution Pattern:

Worldwide Distribution - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden. .

Voluntary or Mandated:

Voluntary: Firm initiated