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LumiQuick Diagnostics Recalls
80 recalls on record · April 16, 2014 to April 16, 2014 · Medical Devices
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls CK-MB Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls CK-MB Test Card (serum); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Myoglobin Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Myoglobin Test Card (Serum); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Cardiac Panel Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Cardiac Panel Test (Serum); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Troponin I test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Troponin I test Card (serum); LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls K2 (synthetic Marijuana) Test card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls K2 (synthetic Marijuana) Test Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Clonazepam Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Fentanyl Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Fentanyl Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Fentanyl Test Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Methylphenidate Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Methylphenidate Test Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Propoxyphene Test Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Propoxyphene Test Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Alcohol Test, Urine; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Oxycodone Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Oxycodone Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Buprenorphine Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Buprenorphine Test Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Ketamine Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Ketamine Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls THC Test Card; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls THC Strip; LumiQuick,. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls PCP Test Card; LumiQuick. Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls PCP Test (Strip); LumiQuick, Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
April 16, 2014Medical DevicesFDA
LumiQuick Diagnostics Inc. recalls Morphine Test Card (2000); LumiQuick, Santa Clara, CA 95054
Hazard: Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.