Data Foundry

Medical device recalls 2014

TRx Vertical Positioner — Class II medical device recall Z-2657-2014

Terminated recall by Motion Concepts, reported 2014-09-24, distributed in AR, CA, CT, DE, IA, ID, IL, IN…. Motion Concepts identified that there is a possibility of knee support failure occurring through fatigue of tw

Recall numberZ-2657-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMotion Concepts, Concord, N/A, Canada
Recall initiated2014-08-28
Classified2014-09-17
Reported by FDA2014-09-24
Terminated2015-06-03
DistributedAR, CA, CT, DE, IA, ID, IL, IN, MD, MI, MO, NE, NY, OH, PA, TN, TX, WA
Quantity59 units
Serial numbers028380, 28583, 28597, 28604, 28607, 28629, 30334, U001050, U001083, U001544, U002020, U002326, U002386, U002403, U002411, U002489, U002502, U002505, U002509, U002510, U002519, U002716, U002922, U003577, U004011 and 35 more

Product

TRx Vertical Positioner, Classification Name: Wheelchair Component - Power Positioning System.

Reason for recall

Motion Concepts identified that there is a possibility of knee support failure occurring through fatigue of two attachment bolts in the Vertical Position System (TRx Vertical Positioner).

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2657-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.