FDA Devices recall · Reported March 4, 2015
Storm Series Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width configurations with power recline seating system and a conventional style back.
If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight may cause the headrest knob or clamp bracket to pinch, damage or cut …
Invacare Corporation recalled Storm Series Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wh… - a moderate-severity action.
Storm Series Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wh… was recalled by Invacare Corporation in March 4, 2015. Reason: If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight…. Check the official notice for the remedy. Verify recall #Z-1139-2015 with the FDA Devices before acting.
The recall
Invacare Corporation issued this moderate-severity FDA Devices recall-If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight….
- Moderate
- severity level
- 525 units
- affected scope
- Class II
- classification
- March 4, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1139-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1139-2015) was formally reported on March 4, 2015, with the manufacturer initiating the action on January 15, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Invacare Corporation is listed as the recalling firm, operating out of Elyria, OH. Federal records list the affected scope as 525.
The documented reason for this recall is: If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight may cause the headrest knob or clamp bracket to pinch, damage or cut the wire. Smoking, sparking, burning … Distribution data in the federal record shows the product reached: Worldwide Distribution-US (nationwide) including DC and the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, U…. 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
Storm Series Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width configurations with power recline seating system and a conventional style back.
Reason for recall
If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight may cause the headrest knob or clamp bracket to pinch, damage or cut the wire. Smoking, sparking, burning or fire may occur if a wire is repetitively pinched at the same place.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1139-2015 |
| Date reported | March 4, 2015 |
| Date initiated | January 15, 2015 |
| Recalling firm | Invacare Corporation |
| Firm location | Elyria, OH |
| Affected scope | 525 |
| Distribution | Worldwide Distribution-US (nationwide) including DC and the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, a… |
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-1139-2015) 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