FDA Device recall Z-2014-2012
Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker
- FDA Device
- Class II
- terminated
- Published 2012-07-25
On 2012-07-25 the FDA classified a Class II recall of Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker by Etac Supply Center Ab, citing the recall has been initiated because there is the potential that users may fall and become injured, with the potential for serious injury, including bone fracture. One death occu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2014-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-06 |
| Published | 2012-07-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Etac Supply Center Ab |
| Distribution | US |
Product
Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker. These products are four-wheeled walkers intended as a walking aid for indoor and outdoor use for persons weighing up to 125 KG.
Reason
The recall has been initiated because there is the potential that users may fall and become injured, with the potential for serious injury, including bone fracture. One death occurred in a user fall incident, but it is unclear whether the fall was caused by the loss of a wheel. Among the walkers distributed worldwide, Etac¿ has received a total of 49 reports from Europe and Japan of wheels falling
Identifiers
| code_info | Model numbers: 15030102-15, 15030103-15 , 15030202-15, 15030403-15 , 15031003-14, 15040105-14, 15040105-33, 15040301-14, 15040301-33, and 15110101-18. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2014-2012%22
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