RegWardenFDA facility compliance records
Company

SECHRIST INDUSTRIES, INC.

2 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2008: 1 recalls; 2015: 1 recalls1’08’09’10’11’12’13’141’15’16’17’18’19’20’21’22’23’24’25’26
  • Recalls (2)

Registered facilities (1)

Recalls & enforcement

  • Class IITerminated2015-06-01
    Sechrist Industries is recalling the Sechrist Low Profile Wheeled Stretcher because it may experience an unexpected incline angle during the height adjustment of the Low Profile Wheeled Stretcher when lifting the patient upward or when lowering the Wheeled Stretcher to a height a…
  • Class IITerminated2008-08-28
    Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “SECHRIST INDUSTRIES, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2020676-sechrist-industries-inc/

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