Reported Dec 30, 2015 · Terminated
iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131
Ameditech Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Ameditech Inc · 9940 Mesa Rim Rd · San Diego, CA · 92121-2910
Is this the product you have?
iCup DX 11 Panel w/ AdulterantItem No. I-DXA-1117-131
- Lot codes and dates
- 152459 152823
- Amount recalled
- 26 units
This recall covers 59 products
The agency filed one notice per product. You are reading one of them; the other 58 are below.
46 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity for up to two (2) of the nineteen (19) Benzodiazepine (BZO) compounds for which specificity information is provided in the product insert. The particular BZO compounds for which there may be reduced reactivity are Clonazepam and Chlordiazepoxide.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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