Z-2281-2018 Class II Terminated
FDA device recall Z-2281-2018 was initiated by Konica Minolta Medical Imaging USA, Inc. on May 9, 2018 and is designated Class II. 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 c… The recall status is terminated (terminated April 10, 2020).
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
CS-7, Model No. A4C1
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.