FDA Devices recall · Reported July 4, 2018
CS-7, Model No. A4C1
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 …
Konica Minolta Medical Imaging USA, Inc. recalled CS-7, Model No. A4C1 - a moderate-severity action.
CS-7, Model No. A4C1 was recalled by Konica Minolta Medical Imaging USA, Inc. in July 4, 2018. Reason: Panasonic has issued a Mandatory Product Safety Notice, indicating a possibility of battery ignition (fire) i…. Check the official notice for the remedy. Verify recall #Z-2281-2018 with the FDA Devices before acting.
The recall
Konica Minolta Medical Imaging USA, Inc. issued this moderate-severity FDA Devices recall-Panasonic has issued a Mandatory Product Safety Notice, indicating a possibility of battery ignition (fire) i….
- Moderate
- severity level
- Class II
- classification
- July 4, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2281-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
The number of affected units is not disclosed in the agency filing, which is common for drug and food recalls where lot-level tracking supersedes unit counts. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 41,021 medical devices recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2281-2018 |
| Date reported | July 4, 2018 |
| Date initiated | May 9, 2018 |
| Recalling firm | Konica Minolta Medical Imaging USA, Inc. |
| Firm location | Wayne, NJ |
| Affected scope | Not disclosed |
| Distribution | Nationwide distribution. Foreign distribution to Argentina, Brazil, Canada, Chile, Colombia, Ecuador, Japan, Mexico, Netherlands, and Peru. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2281-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
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Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026