FDA Recall Terminated

Head Holder shipped with Ingenuity Core Computed Tomography X-ray Systems. Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

Recall: Z-2203-2015 · Initiated March 17, 2015

Recall

Recall Number
Z-2203-2015
Event Number
71227
Firm
Philips Medical Systems (Cleveland) Inc
FEI Number
1525965
Product Code
JAK
Status
Terminated
Root Cause
Mixed-up of materials/components
Initiated
March 17, 2015
Posted
July 22, 2015
Terminated
June 26, 2018
Address
595 Miner Rd, Cleveland, OH, 44143-2131

Description

Head Holder shipped with Ingenuity Core Computed Tomography X-ray Systems. Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

Reason

A head holder released for use with other CT systems but not yet qualified for use on the Ingenuity Core, which was shipped with this system.

Action

On 6/4/2015, the firm mailed Customer Information Letters.

Distribution

Worldwide Distribution-Product was shipped to the following states: AR, AR, AZ, CA, CO, CT, FL, GA, IA, IN, KS, LA, MA, MD, MI, MO, MS, NC, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, VA, VT, WA, WV & WY, and to the following countries: Argentina, Australia, Bangladesh, Belgium, Brazil, Bulgaria, China, Colombia, Denmark, Ecuador, France, Germany, India, Indonesia, Israel, Japan, Latvia, Libya, Myanmar, Norway, Oman, Poland, Republic of Korea, Russian Federation, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, United Kingdom & Viet Nam.

Quantity

79 units