RegWardenFDA facility compliance records
Facility

SMISSON-CARTLEDGE BIOMEDICAL LLC

1 recall(s) on record — most severe on record: Class I.

Activity by year

FDA actions on record by year2018: 1 inspections; 2021: 1 recalls; 2023: 1 inspections2017120182019202012021202212023202420252026
  • Recalls (1)
  • Inspections (2)

Devices registered here (3)

Recalls & enforcement

  • Class ITerminated2021-02-18
    Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

FDA inspections (2)

  • NAI2023-09-15
    No Action Indicated · Compliance: Devices
  • NAI2018-02-28
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

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. “SMISSON-CARTLEDGE BIOMEDICAL LLC (FEI 3006158088) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006158088-smisson-cartledge-biomedical-llc/

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