Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported December 26, 2012
ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors.
The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
ThyssenKrupp Access Corp recalled ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mo… - a moderate-severity action.
ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mo… was recalled by ThyssenKrupp Access Corp in December 26, 2012. Reason: The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable p…. Check the official notice for the remedy. Verify recall #Z-0557-2013 with the FDA Devices before acting.
The recall
ThyssenKrupp Access Corp issued this moderate-severity FDA Devices recall-The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable p….
- Moderate
- severity level
- Class II
- classification
- December 26, 2012
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0557-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0557-2013) was formally reported on December 26, 2012, with the manufacturer initiating the action on August 6, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. ThyssenKrupp Access Corp is listed as the recalling firm, operating out of Grandview, MO. Federal records list the affected scope as 5,413 stairlifts.
The documented reason for this recall is: The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled. Distribution data in the federal record shows the product reached: Worldwide Distribution-USA (nationwide) including the states of IL, IN, MI, OH, WI, IA, KS, MN, MO, NE, SD, AR, LA,OK, TX. AZ, CO, ID, MT, NM, UT, MT, AK, CA, HI, OR, WA, AL, FL, GA, KY, NC, SC, TN, MD, PA, VA, WV, CT…. 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, 3 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 - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
5,413 stairlifts
Related Recalls
6
3 from same agency
Product description
ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors.
Reason for recall
The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0557-2013 |
| Date reported | December 26, 2012 |
| Date initiated | August 6, 2012 |
| Recalling firm | ThyssenKrupp Access Corp |
| Firm location | Grandview, MO |
| Affected scope | 5,413 stairlifts |
| Distribution | Worldwide Distribution-USA (nationwide) including the states of IL, IN, MI, OH, WI, IA, KS, MN, MO, NE, SD, AR, LA,OK, TX. AZ, CO, ID, MT, NM, UT, MT, AK, CA, HI, OR, WA, AL, FL, GA, KY, NC, SC, TN, MD, PA, VA, WV, CT, MA, ME, NH, NJ, NY… |
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-0557-2013) 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.
Frequently Asked Questions
What product was recalled? ▼
ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors.. Recalled by ThyssenKrupp Access Corp. Units affected: 5,413 stairlifts.
Why was this product recalled? ▼
The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 26, 2012. Severity: Moderate. Recall number: Z-0557-2013.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution-USA (nationwide) including the states of IL, IN, MI, OH, WI, IA, KS, MN, MO, NE, SD, AR, LA,OK, TX. AZ, CO, ID, MT, NM, UT, MT, AK, CA, HI, OR, WA, AL, FL, GA, KY, NC, SC, TN, MD, PA, VA, WV, CT, MA, ME, NH, NJ, NY, RI and VT and the countries of Canada, Nova Scotia and British Columbia.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0557-2013) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 26, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.