Z-2209-2014 Class II Terminated

Recalled by Medical Positioning Inc — Kansas City, MO

FDA device recall Z-2209-2014 was initiated by Medical Positioning Inc on July 10, 2014 and is designated Class II. Reason for recall: Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can ca… The recall status is terminated (terminated January 3, 2017). Affected quantity: 2 beds.

Recall Details

Product Type
Devices
Report Date
August 20, 2014
Initiation Date
July 10, 2014
Termination Date
January 3, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2 beds

Product Description

Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1019. Product Usage: Used to conduct syncope examinations.

Reason for Recall

Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.

Distribution Pattern

Worldwide Distribution - US Nationwide in the states of CA, GA, FL, IL, IN, KS, KY, MD, MN, MO, MS, NC, NY, OH, TN, TX, VA and WI.

Code Information

Serial number--803942