Konica Minolta Medical Imaging USA, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2282-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

ImagePilot, Model No. D9MA

Product Classification:

Class II

Date Initiated: May 9, 2018

Date Posted: July 4, 2018

Recall Number: Z-2282-2018

Event ID: 80220

Reason for Recall:

Panasonic has issued a Mandatory Product Safety Notice, indicating a possibility of battery ignition (fire) in CF-C2 "Toughbook" laptops. Since Konica Minolta uses this laptop in some of its product configurations, it notified its customers to utilize a BIOS Utility for the laptops to minimize the risk of an incident while Panasonic develops a final solution.

Status: Terminated

Product Quantity:

Code Information:

All version numbers.

Distribution Pattern:

Nationwide distribution. Foreign distribution to Argentina, Brazil, Canada, Chile, Colombia, Ecuador, Japan, Mexico, Netherlands, and Peru.

Voluntary or Mandated:

Voluntary: Firm initiated