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iScreen Urine Drug Test
Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 06936983197083
1
510(k) clearances
0
Adverse events
1
Recalls
52
Facilities
Description
1T, DOA-A177H-064-b-A3, AMP500/COC150/FTY1/MDMA500/MET500/MOP300/THC50
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-09-30 | Ameditech Inc | Product was released to market without the adulteration strip included in the product. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.