Facility

STRECK LLC

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

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3017953151
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	11710 Peel Circle La Vista, NE, US 68128
Registration status	Active · expires 2026
Parent company	STRECK (owner-operator 1950302)
Brand names	Guardant cfDNA BCT

Activity by year

Recalls (1)

Devices registered here (1)

Blood Collection Device For Cell-Free Nucleic Acid
Product code QMA (opens in a new tab) · Class II · Clinical Chemistry · 21 CFR 862.1676

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.

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 3017953151) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3017953151-streck-llc/

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