The Anspach Effort, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0830-2014)

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 REF: TURQ-434-4 Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.

Product Classification:

Class II

Date Initiated: March 31, 2011

Date Posted: February 5, 2014

Recall Number: Z-0830-2014

Event ID: 67176

Reason for Recall:

Cutter was longer than was stated on the label

Status: Terminated

Product Quantity: 29 cutting burs

Code Information:

Lot #'s: D323038131 and D343038845

Distribution Pattern:

Worldwide Distribution - USA including CA, CO, IN, KY, MD and TX and Internationally to Japan, Taiwan, United Kingdom, Sweden, and Germany.

Voluntary or Mandated:

Voluntary: Firm initiated