Home / Recalls / Konica Minolta Medical Imaging USA, Inc. / Z-2282-2018

Z-2282-2018 Class II Terminated

Recalled by Konica Minolta Medical Imaging USA, Inc. — Wayne, NJ

Recall Details

Product Type
Devices
Report Date
July 4, 2018
Initiation Date
May 9, 2018
Termination Date
April 10, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity

Product Description

ImagePilot, Model No. D9MA

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.

Distribution Pattern

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

Code Information

All version numbers.

Other recalls by Konica Minolta Medical Imaging USA, Inc.

  • Z-2281-2018 Class II — CS-7, Model No. A4C1 (May 9, 2018)
  • Z-1212-2018 Class II — Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 0456014194003 (December 4, 2017)
  • Z-1215-2018 Class II — Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8AR, UDI: 0456014194158 (December 4, 2017)
  • Z-1213-2018 Class II — Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8WA, UDI: 0456014194453 (December 4, 2017)
  • Z-1214-2018 Class II — Sonimage HS1 Ultrasound Kit AC adapter, Product Number: 1. A9RP, UDI: 0456014194 (December 4, 2017)