PlainRecalls
FDA Devices Moderate Class II Terminated

Drill, 2.5x94mm, Stryker, Item Number 502015136

Reported: May 29, 2019 Initiated: April 8, 2019 #Z-1421-2019

Product Description

Drill, 2.5x94mm, Stryker, Item Number 502015136

Reason for Recall

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

Details

Recalling Firm
Zimmer GmbH
Units Affected
N/A
Distribution
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.
Location
Winterthur, N/A

Frequently Asked Questions

What product was recalled?
Drill, 2.5x94mm, Stryker, Item Number 502015136. Recalled by Zimmer GmbH. Units affected: N/A.
Why was this product recalled?
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 29, 2019. Severity: Moderate. Recall number: Z-1421-2019.