RecallRadar

FDA Device recall Z-2014-2012

Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker

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

AgencyFDA Device
Recall numberZ-2014-2012
ClassificationClass II
Statusterminated
Initiated2012-04-06
Published2012-07-25
Last updated2026-09-13 11:53 UTC
CompanyEtac Supply Center Ab
DistributionUS

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_infoModel 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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.