AmediCheck Instant Test Cup — Class III medical device recall Z-2311-2016
Terminated recall by Branan Medical Corporation, reported 2016-08-10, distributed nationwide. Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug cup, because it may erroneously co
| Recall number | Z-2311-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Branan Medical Corporation, Irvine, CA, United States |
| Recall initiated | 2016-07-05 |
| Classified | 2016-08-01 |
| Reported by FDA | 2016-08-10 |
| Terminated | 2016-10-04 |
| Distributed | Nationwide (US) |
| Quantity | 96 units |
| Model numbers | C-C0501A-3A |
Product
AmediCheck Instant Test Cup, Part No. C-C0501A-3A Product Usage: The AmediCheck Instant Test Cup is an in vitro diagnostic test for the rapid detection of the following drugs in human urine. Drug Analyte Cut off Device Code Marijuana THC 50 ng/mL THC Cocaine Benzoylecgonine 300 ng/mL COC Amphetamine Amphetamine 1000 ng/mL AMP Methamphetamine Methamphetamine 1000 ng/mL MET Opiates Morphine 2000 ng/mL OPI Opiates300 Morphine 300 ng/ml OPI300 Phencyclidine Phencyclidine 25 ng/mL PCP Barbiturates Secobarbital 300 ng/mL BAR Benzodiazepines Oxazepam 300 ng/mL BZD Methadone Methadone 300 ng/mL MTD Oxycodone Oxycodone 100 ng/mL OXY MDMA MDMA 500 ng/mL MDMA Tricyclic Antidepressants Nortriptyline 1000 ng/mL TCA
Reason for recall
Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug cup, because it may erroneously contain 12 panel cups due to a packaging error.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.