RegWardenFDA facility compliance records
Facility

Copan Industries, Inc.

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

Activity by year

FDA actions on record by year2013: 1 recalls; 2021: 1 recalls; 2022: 1 inspections; 2025: 2 recalls1’13’14’15’16’17’18’19’201’211’22’23’242’25’26
  • Recalls (4)
  • Inspections (1)

Devices registered here (1)

  • Culture Media, Non-Propagating Transport
    Product code JSM (opens in a new tab) · Class I · Microbiology · 21 CFR 866.2390

Recalls & enforcement

  • Class IIOngoing2025-10-29
    Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
  • Class IIOngoing2025-05-02
    Swabs for specimen collection may be prone to breakage during product usage.
  • Class IITerminated2021-07-09
    A sterility assurance level of 10-6 cannot be guaranteed due to intentional fraud and data integrity issues at the contract sterilizer, Steril Milano.
  • Class IIITerminated2013-08-09
    The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary from the manufacturer in order to eliminate the very low risk…

FDA inspections (1)

  • NAI2022-07-14
    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. “Copan Industries, Inc. (FEI 3015441043) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3015441043-copan-industries-inc/

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