The Anspach Effort, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2294-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

ANSPACH - 4MM x 11 MM Fluted Barrel, 14 Flutes; REF M-4BA-A-G1. Cutting shaping bone including spine and cranium.

Product Classification:

Class II

Date Initiated: April 13, 2015

Date Posted: August 5, 2015

Recall Number: Z-2294-2015

Event ID: 71212

Reason for Recall:

G1 Dissection Tools are not compatible with all attachments listed on the labeling; G1 cutting tools are labeled with a Specified Shaft Exposure which may not be consistent when used with each attachment on the product label. Shaft exposure may be greater.

Status: Terminated

Product Quantity: 92 tools.

Code Information:

REF M-4BA-A-G1 ; ALL lot numbers

Distribution Pattern:

Worldwide Distribution - US including AZ, CA, CO, FL, GA, IL, KY, LA, MN, MO, NC, NJ, NY, OH, OR, PA, TX, and Internationally to Canada and China.

Voluntary or Mandated:

Voluntary: Firm initiated