ImagePilot — Class II medical device recall Z-2282-2018
Terminated recall by Konica Minolta Medical Imaging USA, Inc., reported 2018-07-04, distributed nationwide. Panasonic has issued a Mandatory Product Safety Notice, indicating a possibility of battery ignition (fire) in
| Recall number | Z-2282-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Konica Minolta Medical Imaging USA, Inc., Wayne, NJ, United States |
| Recall initiated | 2018-05-09 |
| Classified | 2018-06-22 |
| Reported by FDA | 2018-07-04 |
| Terminated | 2020-04-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BR, CA, CL, CO, EC, JP, MX, NL, PE |
| Model numbers | D9MA |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2282-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.