Severity
Moderate
FDA Devices recall · Reported July 22, 2015
The Supporter toilet armrest has two Fast Nuts fixing the product to the toilet porcelain. The firm has reports of the two Fast Nuts coming loose and causing the Supporter to beco…
Etac Supply Center Ab recalled Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfo… - a moderate-severity action.
Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfo… was recalled by Etac Supply Center Ab in July 22, 2015. Reason: The Supporter toilet armrest has two Fast Nuts fixing the product to the toilet porcelain. The firm has repor…. Check the official notice for the remedy. Verify recall #Z-2073-2015 with the FDA Devices before acting.
The recall
Etac Supply Center Ab issued this moderate-severity FDA Devices recall-The Supporter toilet armrest has two Fast Nuts fixing the product to the toilet porcelain. The firm has repor….
Sourced from official FDA Devices enforcement records. Verify recall #Z-2073-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-2073-2015) was formally reported on July 22, 2015, with the manufacturer initiating the action on June 15, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Etac Supply Center Ab is listed as the recalling firm, operating out of Anderstorp, N/A. Federal records list the affected scope as 25 units.
The documented reason for this recall is: The Supporter toilet armrest has two Fast Nuts fixing the product to the toilet porcelain. The firm has reports of the two Fast Nuts coming loose and causing the Supporter to become unsteady. Distribution data in the federal record shows the product reached: Nationwide Distribution including GA, CT and PA.. 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.
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.
Severity
Moderate
Affected scope
25 units
Related Recalls
6
3 from same agency
Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfortable rounded grips for the hands. Supporter is simple to mount without the need for any tools. It fits both floor and wall mounted toilets. If space around the toilet is limited either armrest can easily be detached. Supporter includes seat ring and lid.
The Supporter toilet armrest has two Fast Nuts fixing the product to the toilet porcelain. The firm has reports of the two Fast Nuts coming loose and causing the Supporter to become unsteady.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2073-2015 |
| Date reported | July 22, 2015 |
| Date initiated | June 15, 2015 |
| Recalling firm | Etac Supply Center Ab |
| Firm location | Anderstorp, N/A |
| Affected scope | 25 units |
| Distribution | Nationwide Distribution including GA, CT and PA. |
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.
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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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 July 22, 2015. 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.