CLASS II Device recall · Reported 22 Jul 2015 · FDA Enforcement Report
Etac Supporter toilet armrest Etac Supporter toilet recalled
Etac Supply Center Ab is recalling Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have, distributed nationwide in the US. The recall was initiated on 15 Jun 2015 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2073-2015
- FDA event ID
- 71515
- Recalling firm
- Etac Supply Center Ab, Anderstorp, N/A
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 15 Jun 2015
- FDA classified
- 14 Jul 2015
- Reported
- 22 Jul 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 15 Jun 2015 | Recall initiated by company | |
| 14 Jul 2015 | Classified by FDA | +29 days |
| 22 Jul 2015 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Product as listed by the FDA
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.
Where it was distributed
Nationwide Distribution including GA, CT and PA.
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
Serial numbers higher than 224017
Where was it sold?
Nationwide Distribution including GA, CT and PA.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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