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Z-0780-2013 Class II Terminated

Recalled by Winco Mfg., LLC — Ocala, FL

FDA device recall Z-0780-2013 was initiated by Winco Mfg., LLC on Sep 24, 2012 and is designated Class II. 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. The recall status is terminated (terminated May 23, 2013). Affected quantity: 95 units (All models).

Recall Details

Product Type: Devices
Report Date: Feb 13, 2013
Initiation Date: Sep 24, 2012
Termination Date: May 23, 2013
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 95 units (All models)

Product Description

Designer Care Cliner 6700/6704/6710 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.

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.

Distribution Pattern

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

Code Information

Model 6700, 6704 and 6710. Serial numbers: 670A100027, 670A100028, 670A100323, 670100082, 670100083, 670A100101, 670A100021, 670A100324, 670A100325, 670A100284, 670A100242, 670100005, 670100124, 670100125, 670100181, 670100182, 670100183, 670100184, 670100185, 670100186, 670100026, 670A100004, 670A100036, 670A100037, 670A100038, 670A100039, 670A100040, 670A100041, 670A100042, 670A100043, 670A100044, 670A100124, 670A100135, 670A100138, 670A100137, 670A100278, 670A100299, 670A100308, 670A100345, 670A100365, 670A100191, 670A100243, 670A100303, 670100027, 670100193, 670A100244, 670A100245, 670A100246, 670100018, 670100022, 670100021, 670100020, 670100175, 670100176, 670100177, 670100171, 670100187, 670100188, 670100189, and 670100190

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-0780-2013
openFDA file date: Oct 26, 2026
Loaded by RegDataLab: Oct 27, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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