FDA recall Z-0296-2018

Zimmer Biomet, Inc. · Class II · device

Product

Lateral Troch Plate Full Crimp - 254mm, model # 350837

Reason for recall

Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.

Distribution

Nationwide in US; Internationally Argentina, Netherlands & Canada

Key facts

Status
Terminated
Initiation date
2017-06-05
Report date
2018-01-10
Termination date
2018-03-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0296-2018