ToxCup Drug Screen Cup — Class II medical device recall Z-1508-2014
Terminated recall by Branan Medical Corporation, reported 2014-04-30, distributed nationwide. May be labeled with incorrect result interpretation graphics on the ToxCup lid label.
| Recall number | Z-1508-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Branan Medical Corporation, Irvine, CA, United States |
| Recall initiated | 2014-03-26 |
| Classified | 2014-04-24 |
| Reported by FDA | 2014-04-30 |
| Terminated | 2014-07-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 9,800 units |
| Reason classes | labeling |
| Lot numbers | N0854, O0013, O0056, O0057, O0059, O0060, O0067, O0079, O0099, O0100 |
| Model numbers | HT15, HT15A, PT11, PT11A, PT15A, PT23A |
Product
ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A, a screening device for the detection of drugs and drug metabolites in human urine. For in vitro diagnostic use only.
Reason for recall
May be labeled with incorrect result interpretation graphics on the ToxCup lid label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1508-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.