Recall Register

Food, drugs, devices › Etac Supply Center Ab

Device recall: Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt shower chair. Height adjustable four wheele

FDA enforcement event 65401 · Class II · initiated 23 May 2013 · status Terminated · terminated 24 Oct 2014

DeviceVoluntary: Firm initiated1 product recordAnderstorp, N/A

FDA enforcement event 65401 is a device recall by Etac Supply Center Ab of Anderstorp, N/A, initiated 23 May 2013 and classified Class II, with 1 product record.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 90% of the 1,236 device enforcement events initiated in 2013 carry the same class.

Status: Terminated, terminated 24 Oct 2014. Initiation: voluntary: firm initiated. Etac Supply Center Ab has 4 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Etac Supply Center Ab, Anderstorp, N/A, Sweden.

Reason for recall

"Etac is voluntarily conducting a field correction of the Etac Swift Mobil shower chair. If the Swift Mobil shower chair loses a caster and thus becomes instantly unstable, there is potiential risk for harm or injury."

Distribution

"International distribution: Austria, Australia, Belgium, Brazil, Canada, Czech Republic, Denmark, Esonia, Finland, France, Great Britain, Germany, Greece, Hong Kong, Ireland, Isreal, Iceland, Italy,…"

Product records

Recall numberProductQuantityClassStatusReport date
Z-1807-2013Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt shower chair. Height adjustable four wheeled shower chairs for persons of various weights.7200 internationallyClass IITerminated31 Jul 2013

Context

90%of 2013 device events are Class II1,236 events that year
1product record in this eventfirm median: 1
4events on this register for the firm

Other enforcement events for Etac Supply Center Ab

InitiatedProduct (first record)TypeClassRecords
12 Jul 2015Etac Relax wall mounted shower seat The Etac Relax is a wall mounted shower seat designed as a seating and standing suppDeviceClass II1
15 Jun 2015Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfortable rounded grips for the hanDeviceClass II1
6 Apr 2012Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker. These products are four-wheeled walkers intended as a walkDeviceClass II1

All 4 events for Etac Supply Center Ab

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "Etac is voluntarily conducting a field correction of the Etac Swift Mobil shower chair. If the Swift Mobil shower chair loses a caster and thus becomes instantly unstable, there is potiential risk for harm or injury."

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "International distribution: Austria, Australia, Belgium, Brazil, Canada, Czech Republic, Denmark, Esonia, Finland, France, Great Britain, Germany, Greece, Hong Kong, Ireland, Isreal, Iceland, Italy,…"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 24 Oct 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.