PlainRecalls

LumiQuick Diagnostics Inc.

Compiled from official public sources by the editorial team.

80 recalls on record · Latest: Apr 16, 2014

LumiQuick Diagnostics Inc. Recall Insight

LumiQuick Diagnostics Inc. appears on 80 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.079% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Apr 16, 2014, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 30 entries, severity tagging shows 0 critical, 30 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 30 of 30 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (30). The date window on this page runs from Apr 16, 2014 to Apr 16, 2014.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Apr 16, 2014

Troponin I test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Myoglobin Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

K2 (synthetic Marijuana) Test card; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Benzodiazepine Test Card; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Cardiac Panel Test (Serum); LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Fecal Occult Blood Test Card; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Barbiturate Test Card; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

MDMA/Ecstasy Strip; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Malaria pan Antigen Test; LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Fentanyl Test Strip; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Fentanyl Test Card; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

MDMA/Ecstasy Test Card; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Strep A Test Card; LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Amphetamine Test Card; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Buprenorphine Test Card; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Oxycodone Test Card; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Dengue NS1 Antigen Test Card; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Salmonella typhi/paratyphi Antigen Test; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Rickettsia IgG/IgM Test Card LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Cardiac Panel Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

EDDP Strip; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

H. Pylori Antigen Test Card LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Syphilis Test Strip (Serum) LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Myoglobin Test Card (Serum); LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Cocaine Strip; LumiQuick. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Adeno/Rota Combo Test Card; LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

THC Strip; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Alcohol Test, Urine; LumiQuick,. Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

PCP Test (Strip); LumiQuick, Santa Clara, CA 95054

FDA Devices Moderate Apr 16, 2014

Methadone Test Strip; LumiQuick,. Santa Clara, CA 95054

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare LumiQuick Diagnostics Inc. with Zimmer Biomet, Inc. →

Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.