MED-MIZER, INC
3 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (3)
- Inspections (2)
Devices registered here (1)
- Bed, Ac-Powered Adjustable HospitalProduct code FNL (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5100
Recalls & enforcement
- Class IIOngoing2023-02-03Risk 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 IITerminated2018-07-25Under 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 IITerminated2014-04-18All 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…
FDA inspections (2)
- VAI2021-08-06Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- NAI2018-03-28No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “MED-MIZER, INC (FEI 3004976058) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004976058-med-mizer-inc/
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