PlainRecalls

Ameditech Inc

Compiled from official public sources by the editorial team.

109 recalls on record · Latest: Oct 7, 2020

Ameditech Inc Recall Insight

Ameditech Inc appears on 109 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.107% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Oct 7, 2020, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 23 moderate, and 27 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Dec 30, 2015 to Oct 7, 2020.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Oct 7, 2020

First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC); AMT Item Number 990100B

FDA Devices Moderate Oct 7, 2020

Noble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B /"Noble 1 Step + Cup" THC50/COC150; OPI300/MET500; AMP500/BZO300; BAR300/MTD30…

FDA Devices Moderate Oct 7, 2020

ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest Drugs of Abuse Cup AMP1000+BZO300+COC300+OPI2000+THC50 …

FDA Devices Moderate Oct 7, 2020

Drug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number 100163/ EDI OPI (300) Uncut Sheet-Card /187876, 100195/ EDI PPX Uncut …

FDA Devices Moderate Oct 7, 2020

TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA Drugs of Abuse Cup AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, N…

FDA Devices Moderate Oct 7, 2020

Henry Schein One Step + DOA Cup (AMT Item Number/ AMT Description): 570-1066 / "Henry Schein OneStep+ DOA Cup 14 Panel AMP500/BAR/BUPG/BZO/COC150…

FDA Devices Moderate Oct 7, 2020

First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B

FDA Devices Moderate Oct 7, 2020

Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Description): 164-DXA14 /"Consult Diagnostics DRUGS OF ABUSE TEST CUP 14-DRUG PANE…

FDA Devices Moderate Oct 7, 2020

ToxCup Drug Screen Cup (AMT Item Number/ AMT Description): HT29A/"ToxCup¿ Drug Screen Cup COC300/MET500/OPI300/THC50/AMP1000/PCP25/OXY100 Adul…

FDA Devices Moderate Oct 7, 2020

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)+(…

FDA Devices Moderate Oct 7, 2020

First Check 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B

FDA Devices Moderate Oct 7, 2020

QuickTox Drug Screen DipCard(AMT Item/ AMT Description): QT70/ "QuickTox¿ Drug Screen Dipcard 11 Drug Detection: COC300+OPI300+MET500+THC50+AMP100…

FDA Devices Moderate Oct 7, 2020

ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/ "ProScreen" Drugs of Abuse Test (MET1000/OPI2000)+AMP+BZO+COC+THC", PSD-6…

FDA Devices Moderate Oct 7, 2020

First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC); AMT Item Number 990100B

FDA Devices Moderate Oct 7, 2020

Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description): X11-IS1 BUP-DX/ "Alere iScreen" Dx Single Dip Card Single Drug Detection: B…

FDA Devices Moderate Oct 7, 2020

Alere iScreen Multi Drug Detection (AMT Item Number/ AMT Description): X11-IS12-DX / "Alere iScreen" Dx Multi-Drugs of Abuse Dip Test 12 Drug Det…

FDA Devices Moderate Oct 7, 2020

MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G.",…

FDA Devices Moderate Oct 7, 2020

Oratect III Oral Fluid Drug Screen Device (AMT Item Number/ AMT Description): HM12-CE "Oratect¿ III Oral Fluid Drug Screen Device MET25+THC40+COC…

FDA Devices Moderate Oct 7, 2020

MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G. "

FDA Devices Moderate Oct 7, 2020

Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/ "Alere" iCup¿ Dx 10 Drug Detection + Adulteration AMP/BAR/BZO/COC/MET/MDMA…

FDA Devices Moderate Oct 7, 2020

Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Item Number/ AMT Description): MF25/ "Fastect¿ II Drug Screen Dipstick Test Singl…

FDA Devices Moderate Oct 7, 2020

First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B

FDA Devices Moderate Oct 7, 2020

CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): X07-CLIA-SDDT-25 / CLIA Waived" Inc. Single Drug Dipstick Test BUP10, X07-CLI…

FDA Devices Low Dec 25, 2019

QuickTox 5 Panel Drug Screen DipCard

FDA Devices Low Oct 31, 2018

Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid detection of multiple drugs in …

FDA Devices Low May 9, 2018

Alere iScreen Dx Urine Drug Screen Card

FDA Devices Low Sep 6, 2017

Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1 IFU insert. The Alere iScree…

FDA Devices Low Dec 30, 2015

DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D

FDA Devices Low Dec 30, 2015

11 Panel Card (OPI 300) w/Adult, Item No. 71125AA

FDA Devices Low Dec 30, 2015

ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P

FDA Devices Low Dec 30, 2015

ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W

FDA Devices Low Dec 30, 2015

Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OP

FDA Devices Low Dec 30, 2015

Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5

FDA Devices Low Dec 30, 2015

ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W

FDA Devices Low Dec 30, 2015

10-Panel Pipette Drug Screen, Item No. PSP-10M

FDA Devices Low Dec 30, 2015

iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013

FDA Devices Low Dec 30, 2015

BZO Strip Dip Card (300ng/ml)*, Item No. 100170

FDA Devices Low Dec 30, 2015

1 Step 12 Panel Cup, Item No. NBCA-12M-W

FDA Devices Low Dec 30, 2015

ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX

FDA Devices Low Dec 30, 2015

DrugSmart 11 Test Cup, Item No. 61127D

FDA Devices Low Dec 30, 2015

iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023

FDA Devices Low Dec 30, 2015

ProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBU

FDA Devices Low Dec 30, 2015

Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W

FDA Devices Low Dec 30, 2015

ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300

FDA Devices Low Dec 30, 2015

DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D

FDA Devices Low Dec 30, 2015

ProScProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM

FDA Devices Low Dec 30, 2015

ProScreen 10 Panel Dip Card, Item No. PSD-10MOX, PSD-10MOB, PSD-10MMO300

FDA Devices Low Dec 30, 2015

ProScreen 10 Panel Cup, Item No. PSCup-10M

FDA Devices Low Dec 30, 2015

iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016

FDA Devices Low Dec 30, 2015

ProScreen 12 Panel Cup w/Adult., Item No. PSCupA-12M

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Ameditech Inc with Zimmer Biomet, Inc. →

Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.