FDA Device recall Z-2282-2018
ImagePilot, Model No. D9MA
- FDA Device
- Class II
- terminated
- Published 2018-07-04
On 2018-07-04 the FDA classified a Class II recall of ImagePilot, Model No. D9MA by Konica Minolta Medical Imaging Usa, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2282-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-09 |
| Published | 2018-07-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Konica Minolta Medical Imaging Usa |
| Distribution | US |
Product
ImagePilot, Model No. D9MA
Reason
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.
Identifiers
| code_info | All version numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2282-2018%22
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