Devices

Device Recall DrugCheck

  • Modèle / numéro de série
    ITEM CODE LOT # 40900 A900 061610  40901 A901 042310  40901 A901 050310  40901 A901 070610  40901 A901 081710  40901 A901C 072110  40901 A904 042310  30500-A A500 022610  30500-A A500 062910  30575 -A A575 040110  30575-A A575 010510  30575-A A575 040110  30575-A A575 081110  30575-A A575 092010  30575-A A575 122309  30603-A A603 100810  30671-A A671 052410  30671-A A671 091310  30800-A A800 030810  30800-A A800 061610  30800-A A800 080310  30800-A A800 082510  30800-A A800 090210  30802-3A 3A802 033010  30802-3A 3A802 051310  30802-3A 3A802 063010  30802-3A 3A802 073010  30802-3A 3A802 082310  30900-A A900 032310  30900-A A900 051310  30900-A A900 060810  30900-A A900 061610  30900-A A900 071410  30900-A A900 072810  30900-A A900 082410  30900-A A900 100510  30900-A A900 101210  30904-A A904 051710  30950-A A950 052209  30950-A A950 062910  30950-A A950 072110  31102-A A1402 051110  40901C A901C 030310  40901C A901C 051310  40901C A901C 072110  40901C A901C 082310  60410-3A 3A410 040710  60500-A A500 030310  60500-A A500 052810  60500-A A500 060810  60500-A A500 062910  60500-A A500 070910  60500-A A500 092210  60505-A A505 052010  60505-A A505 062910  60524-A A524 112309  60526-A A526 062310  60535-A A535 022310  60535-A A535 070210  60535-A A535 090210  60600-A A600 040110  60600-A A600 050710  60600-A A600 071210  60600-A A600 081310  60602-4A 4A602 042810  60602-4A 4A602 050510  60630-4A 4A630 051110  60630-A A630 080510  60630-A A630 092210  60635-4A 4A635 061610  60640-4A 4A640 041510  60640-4A 4A640 062210  60640-4A 4A640 072110  60640-A A640 071609  60705-4A 4A705 060410  60705-4A 4A705 100510  60709-A A709 120809  60800-6A 6A800 091610  60800-A A800 022610  60800-A A800 060310  60800-A A800 080910  60800-A A800 092210  60801-A A801 062110  60820-A A800 072310  60820-A A820 060110  60820-A A820 062310  60820-A A820 072310  60820-A A820 100510  60903-A A903 052810  60910-A A910 071210  60910-A A910 100610  60921-A A921 100710  60925-A A925 030110  60925-A A925 060110  60925-A A925 080610  60930-A A930 060710  60930-A A930 081110  61020-A A020 032310  61020-A A020 061610  61020-A A020 081310  61023-A A023 051110  61023-A A023 100110  61026-4A 4A026 030310  61026-4A 4A026 090210  61028-3A 3A028 080210  61030-3A 3A030 071210  61030-3A 3A030 081110  61030-3A 3A030 101410  61044-6A 6A044 072810  61052-4A 4A052 072810  61052-4A 4A052 091010  61100-A A100 051310  61100-A A100 062310  61100-A A100 073010  61100-A A100 082510  61204-A A204 050310  61204-A A204 061010  61204-A A204 061610  61204-A A204 092310  61206-4A 4A206 012810  61206-4A 4A206 083010  61206-6A 6A206 051110  61303-A A303 052010  61401-A A401 062110  61401-A A401 070610  61404-A A401 062110  65500-4A 4A500 030510  65500-4A 4A500 050310  65500-4A 4A500 060710  65500-4A 4A500 061510  65500-4A 4A500 062510  65500-4A 4A500 070910  65500-4A 4A500 072810  65500-4A 4A500 100110  70410-4A 4A410 082510  70500-3A 3A500 071610  70500-3A 3A500 091310  70500-A A500 060810  70500-A A500 072610  70500-A A500 092810  70550-A A550 072610  70602-3A 3A602 072310  70602-3A 3A602 080510  70604-6A 6A604 082310  70630-3A 3A630 072910 70640-4A 4A640 071609  70808-6A 6A808 081310  70808-6A 6A808 082610  70910-A A910 082310  70910-A A910 082610
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including AZ, CA,K CT, FL, GA, IL, IA, LA, MD, MA, MN, MS, MO,K MT, NE, NJ, NY, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI, and WY.
  • Description du dispositif
    Drug Check, Distributed by Express Diagnostics Intl Inc., 1550 Industrial Drive, Blue Earth, MN 56013. || Following Cup and Dip product models involved in the recall: || 40900 || 40901 || 30500-A || 30575 -A || 30603-A || 30671-A || 30800-A || 30802-3A || 30900-A || 30950-A || 31102-A || 40901C || 60410-3A || 60500-A || 60505-A || 60524-A || 60526-A || 60535-A || 60600-A || 60602-4A || 60630-A || 60635-4A || 60640-4A || 60705-4A || 60709-A || 60800-6A || 60800-A || 60801-A || 60820-A || 60903-A || 60910-A || 60921-A || 60925-A || 60930-A || 61020-A || 61023-A || 61026-4A || 61028-3A || 61030-3A || 61044-6A || 61052-4A || 61100-A || 61204-A || 61206-4A || 61206-6A || 61303-A || 61401-A || 61404-A || 65500-4A || 70410-4A || 70500-3A || 70500-A || 70550-A || 70602-3A || 70604-6A || 70630-3A || 70640-4A || 70808-6A || 70910-A || In Vitro immunoassay screening device for the qualitative detection of multiple drugs of substances in human urine.
  • Manufacturer
    Express Diagnostics Int'l., Inc.
  • 1 Event

Fabricant

Express Diagnostics Int'l., Inc.
  • Adresse du fabricant
    Express Diagnostics Int'l., Inc., 1550 Industrial Dr, Blue Earth MN 56013-1100
  • Société-mère du fabricant (2017)
    Express Diagnostics Intl Inc.
  • Source
    USFDA

3 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

Device Recall DrugCheck Drugs of Abuse Ketamine Dip Test
  • Modèle / numéro de série
    PC 09077, PC03227, PC03055, PC09293, PC11115, PC08126, PC06276, PC07085, PC06305, and PC08017.
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- US, including the states of CA, NY, MN, and SC; SWEDEN, CANADA, UNITED KINGDOM, and GUATEMALA.
  • Description du dispositif
    DrugCheck Ketamine Dip Test || 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT. || This assay provides only a preliminary analytical test result.
  • Manufacturer
    Express Diagnostics Int'l., Inc.
Device Recall DrugCheck
  • Modèle / numéro de série
    143235 144216 151591 153132 153489
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5
  • Manufacturer
    Ameditech Inc
Device Recall DrugCheck
  • Modèle / numéro de série
    Product Code Lot Number   70801-4 4-801 112210 70801-4 4-801 102910 65500-4A 4A-500 110310  30705 705 112210 60702-6A AUS 6A-702 112910 60702-6A AUS 6A-702 113010 60600-A A600 110310 61205 205 110410 70701-4 4-701 102910 31012-6 6-012 110310 31003 003 102510
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution: USA (nationwide) including states of: FL, IA, MD, OK, and WA; and countries including: AUSTRALIA and ITALY.
  • Description du dispositif
    DrugCheck, Manufactured by: Express Diagnostics Int;l Inc. 1550 Industrial Drive, Blue Earth MN 56013 USA, Model numbers : || 70801-4(NxScan OnSite, AMP500-COC-MDMA-MET500-MTD-OP1300-TCH-BUP-pH,SG-NI,CR, Lot 4-801 102910, Exp APR 2012, & Lot 4-801 112210, Exp MAY 2012, Export Only); || 65500-4A (AMP-COC--OP1-TCH-MET-ALC-pH,SG-NI,CR, Lot 4A-500 110310, Exp MAY 2012, For forensic use only); || 30705 ( DIP DRUG TEST, AMP500/COC/MDMA/MET500/MTD/OP1300/TCH, Lot 705 112210, Exp MAY 2012); || 60702-6A AUS (AMP300-COC300-OP1300-OP12000-MET300-TCH50-BZ0200-ALC-pH,SG,OX-NI,CR-GL, Lot 6A-702 113010 & 6A-702 112910, Exp MAY 2012, Export Only); || 60600-A (AMP-COC--OP1-TCH-MET-BZO-ALC, Lot A600 110310, Exp MAY 2012, For forensic use only); || 61205 (AMP-BAR-BZO-COC-MDMA-MET-MTD-OPI-OXY-PCP-TCA-THC, Lot 205 110410, Exp MAY 2012); || 70701-4 (NxScan OnSite, AMP500-COC-MDMA-MET500-MTD-OP1300-TCH-pH,SG-NI,CR, Lot 4-701 102910, Exp APR 2012, Export Only); || 31012-6 (DIP DRUG TEST, AMP/BAR/BZO/COC/MDMA/MTD/OPI/OXY/ PCP/THC/pH SG, OX/NI, CR, GL, Lot 6-012 110310, Exp MAY 2012); || 31003 (AMP/COC/OP10300/THC/MET/BZO/BAR/PCP/MTD/TCA/MET, Lot 003 102510, Exp APR 2012); || Intended use: The DrugCheck Dip Drug Test is a one-step immunoassay for the qualitative detection of multiple drugs and drug metabolites in human urine.
  • Manufacturer
    Express Diagnostics Int'l., Inc.