RegWardenFDA facility compliance records
Recall

Class II — Summit Industries Inc.

Recalling firmSUMMIT INDUSTRIES, LLC
Registered facilitySUMMIT INDUSTRIES, LLC (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonThe welds on J700 tube stands may be insufficient resulting in tube stand breakage, damage to the X-Ray machine, and/or patient or healthcare provider injury.
ProductThe J700 Floor Mounted Tube Stand (FMTS) is intended to support and position the diagnostic x-ray tube housing assembly for a medical radiographic procedure. The product consists of a vertical column (with counterbalanced vertical carriage, counterweight and pulley system), horizontal floor car and a floor mounted track to ride on.
Quantity32
DistributionUS Distribution including the states of: AZ, CO, IL, KY, LA, NE, NY, OH, PA, TN, TX, VA, WA and WV.
Initiated2014-10-28
Classified2014-11-26
Terminated2015-05-21
Recall numberZ-0468-2015
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 — Summit Industries Inc. (Z-0468-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69631/

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