Carestream Health, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0126-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Carestream DRX-Revolution Mobile X-ray System. Produces radiographic images.

Product Classification:

Class II

Date Initiated: June 6, 2013

Date Posted: November 6, 2013

Recall Number: Z-0126-2014

Event ID: 65469

Reason for Recall:

Carestream Health Inc. is recalling the power plug on their DRX-Revolution Mobile X-Ray System due to the item generating sparks and becoming warm to touch.

Status: Terminated

Product Quantity: 180 units

Code Information:

Serial Numbers: 111, 114, 119-123, 125-126, 134, 142-143, 151-155, 161-169, 173-178,180-183, 188-192, 196-209, 211, 221-232, 235-249, 254, 261-270, 275-276, 279-286, 305, 312, 316-326, 330-337, 339-349, 353, 355, 357-365, 372-373, 375-376, 379-385, 387-388, 394-401, 403-405, 409-410, 412-415, 417, 420-421, 423, 431-435, 441-446, 451-461, 464-470, and 482-490

Distribution Pattern:

Nationwide Distribution including the states of NY, TX, PA, OH, WI, CA, IL, CO, FL, IN, OK, NJ, GA, LA, AL, KS, AZ, MA, SC, MI, NC, IA, UT, VA, TN, and MN.

Voluntary or Mandated:

Voluntary: Firm initiated