RegWardenFDA facility compliance records
Company

MED-MIZER, INC

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

Recalls by year

FDA actions on record by year2014: 1 recalls; 2018: 1 recalls; 2023: 1 recalls1’14’15’16’171’18’19’20’21’221’23’24’25’26
  • Recalls (3)

Registered facilities (1)

Recalls & enforcement

  • Class IIOngoing2023-02-03
    Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.
  • Class IITerminated2018-07-25
    Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made
  • Class IITerminated2014-04-18
    All configurations of the SS Retractabed, Clinical Contour, made prior to June 7, 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support rails together when using the foot side rails and keeps them from separating fr…

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. “MED-MIZER, 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-9057047-med-mizer-inc/

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