3,190 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TDX/TDXFLX CANNABINOIDS REAGENT
FDA Adverse Event
Injury
·ABBOTT HEALTH PRODUCTS, INC.·Product code LDJ·November 8, 2006
ONLINE DAT CANNABINOIDS II
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LDJ·March 31, 2026
MULTI DRUG 6 PANEL CUP
FDA Adverse Event
Malfunction
·ABON BIOPHARM (HANGZHOU) CO., LTD·Product code LDJ·February 24, 2015
Multi-Drug iCup Drug Screen Test Cup. Part Number DUE-1127-022-08A. Subsequent Product Codes: DIO, DIS, DJC, DJG, DJR, JXM, JXN, LCM, LDJ, LFG
FDA Recall
Terminated
·Biosite Inc·Product code DKZ·April 27, 2009
Multi-Drug iCup Drug Screen Test Cup. Part Number DUD-1107-012-08A. Subsequent Product Codes: DIO, DIS, DJC, DJG, DJR, JXM, JXN, LCM, LDJ, LFG
FDA Recall
Terminated
·Biosite Inc·Product code DKZ·April 27, 2009
Multi-Drug iCup Drug Screen Test Cup. Part Number DUD-197-014-08A. Subsequent Product Codes: DIO, DIS, DJC, DJG, DJR, JXM, JXN, LCM, LDJ, LFG
FDA Recall
Terminated
·Biosite Inc·Product code DKZ·April 27, 2009
Multi-Drug 8 Panel Integrated iCup Drug Screen Test Cup. Part Number DUD-187-013-08A. Subsequent Product Codes: DIO, DIS, DJC, DJG, DJR, JXM, JXN, LCM, LDJ, LFG
FDA Recall
Terminated
·Biosite Inc·Product code DKZ·April 27, 2009
Multi-Drug 8 Panel Integrated iCup Drug Screen Test Cup. Part Number DUE-187-071-08A. Subsequent Product Codes: DIO, DIS, DJC, DJG, DJR, JXM, JXN, LCM, LDJ, LFG
FDA Recall
Terminated
·Biosite Inc·Product code DKZ·April 27, 2009
Enzyme Immunoassay, Cannabinoids
FDA classification
FDA Class 2
·Enzyme Immunoassay, Cannabinoids
Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Description): 164-DXA14 /"Consult Diagnostics DRUGS OF ABUSE TEST CUP 14-DRUG PANEL WITH ADULTERANTS AMP500/BAR/BUPG/BZO/COC150/MDMA/MET500/MOP/MTD/OXY/PCP/PPX/TCA/THC (Bl, Cr, Ni, pH, SG)",
FDA Recall
Terminated
·Ameditech Inc·Product code LDJ·August 18, 2020
Cannabinoids Intercept Micro Plate EIA 100 plate kit
FDA Recall
Terminated
·OraSure Technologies, Inc.·Product code LDJ·September 8, 2008
Micro Plate EIA Oral Fluid Negative Control which is a component of the Intercept Micro Plate EIA kit.
FDA Recall
Terminated
·OraSure Technologies, Inc.·Product code LDJ·September 8, 2008
Oratect III Oral Fluid Drug Screen Device (AMT Item Number/ AMT Description): HM12-CE "Oratect III Oral Fluid Drug Screen Device MET25+THC40+COC20+AMP25+OPI10+BZO5 "
FDA Recall
Terminated
·Ameditech Inc·Product code LDJ·August 18, 2020
SPICE (JWH-018) CC443
FDA Recall
Terminated
·Carolina Liquid Chemistries Corp·Product code LDJ·February 10, 2020
Micro Plate EIA Oral Fluid Cutoff Calibrator which is a component of the Intercept Micro Plate EIA kit.
FDA Recall
Terminated
·OraSure Technologies, Inc.·Product code LDJ·September 8, 2008
AT HOME MARIJUANA TEST STRIP, SKU 900752
FDA Recall
Open, Classified
·Family Dollar Stores, Llc.·Product code LDJ·October 4, 2023
Noble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B /"Noble 1 Step + Cup" THC50/COC150; OPI300/MET500; AMP500/BZO300; BAR300/MTD300; BUPG10/TCA1000; MDMA500/OXY100; w/ Cr, Ni, pH, Bl, S.G. Finished Devices", NBCA-14A-PP/"Noble 1 Step + Cup" (THC50/COC150)+(OPI300/MET500)+ (AMP500/BZO300)+(BAR300/MTD300)+ (BOPG10/TCA1000)+(MDMA500/OXY100)+ (PCP25/PPX300) w/ Cr, Ni, pH, Bl, S.G."
FDA Recall
Terminated
·Ameditech Inc·Product code LDJ·August 18, 2020
AT HOME MARIJUANA TEST STRIP, SKU 900752
FDA Recall
Open, Classified
·Family Dollar Stores, Llc.·Product code LDJ·June 23, 2022
iCup Dx14 Drug Screen Cup(AMT Item Number/ AMT Description): X11-I-DXA-2147-011/ "iCup" Dx 14 Drug Screen Cup 14 Drug Detection: (THC50/COC150)+(MOP300/MET500)+(AMP500/BZO300)+ (BAR300/MTD300)+(BUPG10/TCA1000)+(MDMA500/OXY100)+(PCP25/PPX300) 5 Adulteration Tests: Cr, Ni, pH, Bl, S.G.", X11-I-DX-1147-022 /"iCup" Dx 14 Drug Screen Cup 14 Drug Detection: (THC50/COC150)+(MOP300/MET500)+(AMP500/BZO300)+ (BAR300/MTD300)+(BUPG10/TCA1000)+(MDMA500/OXY100)+(PCP25/PPX300)"
FDA Recall
Terminated
·Ameditech Inc·Product code LDJ·August 18, 2020
First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B
FDA Recall
Terminated
·Ameditech Inc·Product code LDJ·August 18, 2020