FDA recall Z-2245-2019

BioPro, Inc. · Class II · device

Product

K-Wire Single Trocar 2.5x150mm, Item Number OL15025S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

Reason for recall

Manufacturing flaw in the sterile barrier system

Distribution

Worldwide distribution - US Nationwide distribution in the states of FL, LA, MD, NC, NY, OR & TX, and countries of Ecuador, Scotland.

Key facts

Status
Terminated
Initiation date
2019-06-25
Report date
2019-08-21
Termination date
2020-05-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Port Huron, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2245-2019