Zimmer GmbH: Medical Device Recall in 2019 - (Recall #: Z-1446-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Drill, cannulated, 3.5x90mm, round shaft, Item Number 502015635

Product Classification:

Class II

Date Initiated: April 8, 2019

Date Posted: May 29, 2019

Recall Number: Z-1446-2019

Event ID: 82642

Reason for Recall:

An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.

Status: Terminated

Product Quantity: N/A

Code Information:

All items marked with "Normed" are affected

Distribution Pattern:

The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY.

Voluntary or Mandated:

Voluntary: Firm initiated