RegWardenFDA facility compliance records
Recall

Class III — Clarity Diagnostics Llc

Recalling firmClarity Diagnostics
Registered facilityClarity Diagnostics, LLC (the firm's only registered facility)
ClassificationClass III
StatusTerminated
ReasonClarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are not compatible for use in the Clarity Urocheck 120 Urine Analyzers, due to lack of Canister Code Bar Code Label.
ProductClarity Urocheck 10SG Urinalysis Strips, Model # DTG-10SG Product Usage: Clarity 10SG Urinalysis Reagent Strips (Urine) are for the qualitative and semi-quantitative detection of the following analytes in urine: Glucose, Bilirubin, Ketone (Acetoacetic acid), Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite and Leukocytes. The Clarity Urinalysis Reagent Strips (Urine) are for single use in professional near-patient (point-of-care) and centralized laboratory locations, and are intended for professional use only. The strips are intended for use in screening at-risk patients to assi…
Quantity7536 Bottles
DistributionWorldwide Distribution - US Nationwide in the states of AZ, MA, SC, WA. and the country of Austria.
Initiated2018-06-22
Classified2018-08-11
Terminated2024-01-12
Recall numberZ-2786-2018
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class III recall — Clarity Diagnostics Llc (Z-2786-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80535/

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