AtriCure, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1148-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a conventional thermoformed polyethylene terephthalate glycol (PETG) tray with a Tyvek¿ lid. A single-walled non-corrugated box completes the single unit package. Six (6) single unit PRO2 devices are packaged into one (1) corrugate shipper box.

Product Classification:

Class II

Date Initiated: November 30, 2016

Date Posted: February 15, 2017

Recall Number: Z-1148-2017

Event ID: 76017

Reason for Recall:

A complaint of the PRO2 jaw breaking prior to surgery being performed.

Status: Terminated

Product Quantity: 464 units

Code Information:

Model Numbers: PRO235, PRO240, PRO245, PRO250 Lot Numbers: 67102 to 68418

Distribution Pattern:

Devices were distributed in the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NE, NY, OH, OK, PA, SC, TN, TX, UT, VA, VT, & WI. Devices were distributed in the following countries: Austria, Germany, Netherlands, Poland, Sweden, Switzerland and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated