Zimmer, Inc.: Medical Device Recall in 2014 - (Recall #: Z-2217-2014)

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:

Double Offset Rasp Handle, Left Hand Nonsterile

Product Classification:

Class II

Date Initiated: July 23, 2014

Date Posted: August 20, 2014

Recall Number: Z-2217-2014

Event ID: 68656

Reason for Recall:

The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.

Status: Terminated

Product Quantity: 412 units

Code Information:

Item Number 82016757830 Lot Number 97009559

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including the states of AK, AL, AZ, CA, CO, FL, GA, IN, KS, KY, MI, MN, NC, NJ, NY, OH, OK, OR, PA, SD, TN, TX, UT, and VA, and the countries of Australia, France, Germany, Italy, Switzerland, and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated