RegWardenFDA facility compliance records
Facility

STRECK LLC

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

Activity by year

FDA actions on record by year2017: 1 recalls, 1 inspections; 2018: 1 inspections220171201820192020202120222023202420252026
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2017-02-23
    Complaints of the 2.0ml tube stopper coming loose during phlebotomy when small diameter tube adapters were not utilized. Such adapters aid with centering small diameter tubes to properly pierce the middle of the stoppers.

FDA inspections (2)

  • NAI2018-09-20
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
  • NAI2017-11-10
    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. “STRECK LLC (FEI 1950302) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1950302-streck-llc/

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