CLASS II Device recall · Reported 13 Feb 2013 · FDA Enforcement Report

Premier Care Recliner 5570/5574 With Cal Tb 133 Upgrade recalled

Winco Mfg is recalling Premier Care Recliner 5570/5574 With Cal Tb 133 Upgrade Purchased Jan 01, 2011 To August, distributed nationwide in the US. The recall was initiated on 24 Sep 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel 5570 and 5574. Serial numbers: 557A100080, 557A100081, 557100004, 557100008, 557100009, 557100012, 557100041, 557100042, 557100043, 557100044, 557100045, 557A100065, 557100036, 557100037, 557100038, 557100039, 557A100073, and 557100048
Quantity recalled95 units (All models)

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-0778-2013
FDA event ID
63651
Recalling firm
Winco Mfg, Ocala, FL
Classification
Class II
Status
Terminated
Recall initiated
24 Sep 2012
FDA classified
4 Feb 2013
Reported
13 Feb 2013
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons

Timeline

24 Sep 2012Recall initiated by company
4 Feb 2013Classified by FDA+133 days
13 Feb 2013Published in enforcement report+9 days

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

Reason for recall

The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other states.

Product as listed by the FDA

PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.

Where it was distributed

Nationwide Distribution including CA, FL, IL, MA, MD, MN, NM, NY, OH, OK, and TX.

Nationwide CaliforniaFloridaIllinoisMassachusettsMarylandMinnesotaNew MexicoNew YorkOhioOklahomaTexas

Stores named: WinCo

Questions about this recall

Why was it recalled?

The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other states.

Which lots are affected?

Model 5570 and 5574. Serial numbers: 557A100080, 557A100081, 557100004, 557100008, 557100009, 557100012, 557100041, 557100042, 557100043, 557100044, 557100045, 557A100065, 557100036, 557100037, 557100038, 557100039, 557A100073, and 557100048

Where was it sold?

Nationwide Distribution including CA, FL, IL, MA, MD, MN, NM, NY, OH, OK, and TX.

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

3 other products · FDA event 63651

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