Lumiquick Diagnostics recalls
Lumiquick Diagnostics appears in 80 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Drugs of Abuse Panel Test Device
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Ketamine Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Salmonella typhi Antigen Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - THC Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Morphine Test Card (300)
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Methylphenidate Test Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - H. Pylori Antigen Test Card LumiQuick, Santa Clara, CA 95054
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Clonazepam Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - PSA Test Card (Whole Blood)
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Strep A Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Oxycodone Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Syphilis Test Strip (Serum) LumiQuick, Santa Clara, CA 95054
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Dengue NS1 Ag/IgG/M Ab Duo Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Troponin I test Card (serum)
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Myoglobin Test Card (Whole Blood)
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Barbiturate Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Fentanyl Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - MDMA/Ecstasy Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - PCP Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Benzodiazepine Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Amphetamine Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Benzodiazepine Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Rickettsia IgG/IgM Test Card LumiQuick, Santa Clara, CA 95054
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Methamphetamine Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Tramadol Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Tramadol Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Malaria pf Antigen Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Methadone Test Card
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - Salmonella typhi/paratyphi Antigen Test
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance. - MDMA/Ecstasy Strip
FDA Device · Class II · 2014-04-16 · Lumiquick Diagnostics
Reason: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.