3,190 results · 39ms · Sources: EU EUDAMED, 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