Carestream Health, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0844-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

KODAK DirectView DR 7500 Dual Detector System, MODEL DR 7500, Manufactured by Carestream Health, Inc. Made in U.S.A.

Product Classification:

Class II

Date Initiated: December 26, 2013

Date Posted: February 5, 2014

Recall Number: Z-0844-2014

Event ID: 67188

Reason for Recall:

Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing Version 5.X Software due to a possible patient image display error.

Status: Terminated

Product Quantity: 164 units Total (42 domestically & 122 internationally)

Code Information:

Service Code: 8087; Catalog numbers: 8791345, 1155118, 1295088, 8551046, 8791345, 1666700, 8531675

Distribution Pattern:

worldwide Distribution - US (Nationwide) including states of: IN, PA, MD, MI, NY, GA, MN, OK, VA, TX, WI, CA, IL, TN, WA, NC, SC, MA, NJ, and KY; and Internationally to: Canada, New Zealand, South Korea, Australia, Hong Kong, Saudia Arabia, Guinea, Kuwait, Israel, Oman, South Africa, China, UK, Sweden, Poland, Denmark, Germany, Finland, Czech Republic, Italy, France, Portugal and Spain.

Voluntary or Mandated:

Voluntary: Firm initiated