CLASS II Device recall · Reported 26 Aug 2015 · FDA Enforcement Report

Winco Designer Care Cliner w/Swing Arms recalled by Winco Mfg

Winco Mfg is recalling Winco Designer Care Cliner w/Swing Arms - with Nylon Casters Oncology, Dialysis, Hospital, distributed nationwide in the US. The recall was initiated on 2 Apr 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel Number: 6740
Quantity recalled1 chairs

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-2399-2015
FDA event ID
71496
Recalling firm
Winco Mfg, Ocala, FL
Classification
Class II
Status
Terminated
Recall initiated
2 Apr 2015
FDA classified
14 Aug 2015
Reported
26 Aug 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

2 Apr 2015Recall initiated by company
14 Aug 2015Classified by FDA+134 days
26 Aug 2015Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.

Product as listed by the FDA

Winco Designer Care Cliner w/Swing Arms - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.

Where it was distributed

Nationwide Distribution including CA, FL, KS, KY, LA, MA, MD, MN, MS, NJ, NY, OK, TN, TX, and WA.

Nationwide CaliforniaFloridaKansasKentuckyLouisianaMassachusettsMarylandMinnesotaMississippiNew JerseyNew YorkOklahomaTennesseeTexasWashington

Stores named: WinCo

Questions about this recall

Why was it recalled?

Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.

Which lots are affected?

Model Number: 6740

Where was it sold?

Nationwide Distribution including CA, FL, KS, KY, LA, MA, MD, MN, MS, NJ, NY, OK, TN, TX, and WA.

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.

Other products in this recall event

12 other products · FDA event 71496

This product is part of a recall event; the main page for the event is Winco Care Cliner Standart - Steel Casters Oncology recalled.

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