Ameditech Inc recalls
Every recall we track for Ameditech Inc — 27 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Ameditech Inc peaked in 2020 (23); 27 since 2017.
All FDA recall records for Ameditech Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 3 | 0 | 3 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 22 | 1 | 23 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Ameditech Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Ameditech Inc recalls
5 shown- Lower riskMedical device
Ameditech Inc recalls First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC); AMT Item Number 990100B
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.
AmeditechAug 18, 2020 - Lower riskMedical device
Ameditech Inc recalls QuickTox 5 Panel Drug Screen DipCard
Ameditech recalls QuickTox 5 Panel Drug Screen DipCard (P/N QT11, Lot 188787) due to potential false results. Affected users should contact for replacement.
AmeditechFeb 15, 2019 - Lower riskMedical device
Ameditech Inc recalls Alere iScreen Dx Urine Drug Screen Card
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.
AmeditechDec 15, 2017 - Lower riskMedical device
Ameditech Inc recalls Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid
Ameditech recalls Accutest Drug Test Cup 5+3 due to missing adulteration strip. This could lead to inaccurate test results. Affected units have part number DS84S625 and lot number 174886 (US distribution only).
AmeditechSep 30, 2017 - Lower riskMedical device
Ameditech Inc recalls Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1
Ameditech recalls Alere iScreen Dx Urine Drug Screen Cards due to incorrect labeling of PCP instead of TCA in the kit. This may cause misidentification of drugs in urine tests.
AmeditechJun 26, 2017
Ameditech Inc recall questions
How many recalls has Ameditech Inc had?
27 recalls from Ameditech Inc are on record with U.S. safety agencies, from 2017–2020.
What is the most recent Ameditech Inc recall?
Ameditech Inc recalls First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC); AMT Item Number 990100B, dated Aug 18, 2020. Every Ameditech Inc recall is listed on this page, newest first.
What should I do if I have a recalled Ameditech Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Ameditech Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.