RecallRadar

FDA Device recall Z-0312-2016

Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5

On 2015-11-25 the FDA classified a Class II recall of Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5 by Ameditech, citing ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0312-2016
ClassificationClass II
Statusterminated
Initiated2015-10-20
Published2015-11-25
Last updated2026-09-13 11:53 UTC
CompanyAmeditech
DistributionUS

Product

Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5; Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP; Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-12BUP; Immutest 5 panel, Item No. IMCA-5AB-W; Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W; Immutest 7 panel, Item No. IMCA-7P; ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips, including Benzodiazepine (BZO). They are used to obtain a visual, qualitative result and are intended for professional and point of care use. ¿¿¿

Reason

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Identifiers

code_info144380 144564 150505 150908 151538 142098 144103 150313 150909 141645 144563 150483 151337 142076 142966 144263 151540

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0312-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.