Every recall we track for Ameditech Inc — 27 in all — plus the complaints and injury reports the public filed about them.
CLIA Waived recalls certain rapid drug test kits that may not consistently detect drugs due to enzyme failures. Affected products include specific dipstick tests and rapid drug test cups with model numbers X07-CLIA-SDDT-25, X07-CLIA-14-RDTC-A, etc. No remedy is provided in the recall notice.
Ameditech recalls First Check 1 Panel Drug Cup (AMT 990: All lots within expiry) due to inconsistent drug detection. Consumers should contact for remedy.
Ameditech recalls Fastect II drug screen dipsticks that may not consistently detect all drugs due to enzyme failures. Users should stop using affected models to avoid inaccurate results.
Alere iCup Drug Detection products may not consistently detect drugs due to enzyme failure. Affected units include specific model numbers and lots within expiry dates. Consumers should contact the manufacturer for details.
Ameditech recalls MicroScreen devices that may not consistently detect calibrators and compounds due to enzyme failure. Affected units include all lots within expiry date.
Ameditech recalls Oratect III oral fluid drug screening devices due to potential false positive results. Affected units include all lots within expiry date. Consumers should contact Ameditech for details.
Ameditech recalls MicroTox test kits that may not consistently detect all contaminants due to enzyme failures. Affected kits include specific model numbers with chromium, nickel, pH, and other components.
Alere iScreen multi-drug detection tests (X11-IS12-DX, X11-IS10BUP-DX, X11-IS10-DX, X11-IS5 M-DX) may not consistently detect drugs due to enzyme failure. Consumers should stop using affected models.
Alere iScreen single drug detection kits may not consistently detect all drugs due to enzyme failures. Affected kits include Buprenorphine, Barbiturate, Oxycodone, and other drug tests. Consumers should check their kit's model number and expiry date.
Ameditech recalls First Check 4 Panel Drug Cups due to inconsistent detection of calibrators and compounds, potentially leading to inaccurate drug test results.
Ameditech recalls ProScreen drug test kits due to inconsistent detection of calibrators and compounds. Products may not reliably identify drugs as labeled. Consumers should check model numbers and lot dates for affected items.
Ameditech recalls QuickTox Drug Screen DipCards QT70, QT88, QT11, QT52, QT44, QT23, QT80F, QT52A, and QT20 due to inconsistent drug detection results from enzyme failures in immunoassay.
Ameditech recalls First Check 2 Panel Drug Cup (THC/COC) due to inconsistent detection of drugs. All lots within expiry are affected. Consumers should contact for remedy.
Ameditech recalls iCup Dx14 Drug Screen Cups due to inconsistent drug detection results. Products may fail to detect calibrators and secondary compounds as labeled.
Ameditech recalls ToxCup Drug Screen Cups due to inconsistent detection of drugs in tests. Products may fail to detect calibrators and compounds as labeled, risking inaccurate results.
Ameditech recalls 14-drug abuse test cups due to inconsistent drug detection results. Products may fail to detect calibrators and compounds as labeled, risking inaccurate drug screening.
Ameditech recalls 14-panel drug cups due to inconsistent detection of calibrators and compounds, affecting accuracy in drug testing. All lots within expiry are affected.
Henry Schein recalls OneStep+ DOA Cup 14 Panel due to immunoassay enzymes failing to consistently detect all calibrators and compounds as labeled. Affected units may not provide accurate results for drug testing.
Ameditech recalls TDDA Drugs of Abuse Cups due to inconsistent drug detection. Products may not reliably identify all calibrators and compounds as labeled.
Ameditech recalls drug screening sheets that may not consistently detect drugs due to enzyme failures. Affected products include specific lot numbers and catalog codes.
Ameditech recalls ImmuTest Drugs of Abuse Cups due to inconsistent drug detection results. Products may fail to detect all calibrators and compounds as labeled, risking inaccurate test outcomes.
Ameditech recalls Noble 1 Step+ Cup devices due to inconsistent calibrator and compound detection. Products may not detect all substances as labeled. No remedy specified in recall notice.
Ameditech recalls First Check 7 Panel Drug Cup (AMP/COC/MDMA/MET/OPI/PCP/THC) due to inconsistent drug detection. All lots within expiry are affected.
Ameditech recalls QuickTox 5 Panel Drug Screen DipCard (P/N QT11, Lot 188787) due to potential false results. Affected users should contact for replacement.
Ameditech recalls Alere iScreen Dx Urine Drug Screen Cards due to incorrect labeling of drug analytes. This could lead to misidentification of Tricyclic Antidepressants as Phencyclidine (PCP) in test results.
