FDA Devices recall · Reported March 11, 2015
The I-Cart is used to store, transport, and power video equipment used in medical procedures.
The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis.
Richard Wolf Medical Instruments Corp. recalled The I-Cart is used to store, transport, and power video equipment used in medical procedu… - a moderate-severity action.
The I-Cart is used to store, transport, and power video equipment used in medical procedu… was recalled by Richard Wolf Medical Instruments Corp. in March 11, 2015. Reason: The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke an…. Check the official notice for the remedy. Verify recall #Z-1240-2015 with the FDA Devices before acting.
The recall
Richard Wolf Medical Instruments Corp. issued this moderate-severity FDA Devices recall-The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke an….
- Moderate
- severity level
- Class II
- classification
- March 11, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1240-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1240-2015) was formally reported on March 11, 2015, with the manufacturer initiating the action on December 10, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Richard Wolf Medical Instruments Corp. is listed as the recalling firm, operating out of Vernon Hills, IL. Federal records list the affected scope as 83 carts.
The documented reason for this recall is: The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope 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 - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 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
The I-Cart is used to store, transport, and power video equipment used in medical procedures.
Reason for recall
The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1240-2015 |
| Date reported | March 11, 2015 |
| Date initiated | December 10, 2014 |
| Recalling firm | Richard Wolf Medical Instruments Corp. |
| Firm location | Vernon Hills, IL |
| Affected scope | 83 carts |
| Distribution | Nationwide |
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-1240-2015) 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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Methodology · Corrections · Archive as of August 2026