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Recall

Class II — Medical Positioning Inc

Recalling firmMedical Positioning, Inc.
Registered facilityMEDICAL POSITIONING, INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonExcessive 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.
ProductMedical Positioning Rapid Response HUT table with Dual 2 Way Drop Section, Powered Medical Examination table, Model # 1217. Product Usage: Used to conduct syncope examinations.
Quantity17 beds
DistributionWorldwide 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.
Initiated2014-07-10
Classified2014-08-13
Terminated2017-01-03
Recall numberZ-2210-2014
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Medical Positioning Inc (Z-2210-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68763/

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