Drug recall

10-Panel Pipette Drug Screen, Item No. PSP-10M These Drugs of Abuse Tests are one-step immunoassays for the…

FDA recall event 72471 · Class II · Ameditech Inc

Key facts

Event ID 72471
Recall numbers Z-0298-2016, Z-0299-2016, Z-0300-2016, Z-0301-2016, Z-0302-2016, Z-0303-2016, Z-0304-2016, Z-0305-2016, Z-0306-2016, Z-0307-2016, Z-0308-2016, Z-0309-2016 and 8 more
Recalling firm Ameditech Inc
Product type Devices
Products 10-Panel Pipette Drug Screen, Item No. PSP-10M These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The…, 11 Panel Cup (OPI2000) w/Adult, Item No. 71125AA2K ; and 11 Panel Cup (OPI300) w/Adult, Item No. 71125AA These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple…, 11 Panel Dip Card (OPI 2000), Item No. 11125AA2K; 11 Panel Dip Card (OPI 300) w/Adult, Item No. 11125AA These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple…, 12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine…, 1 Step 12 Panel Cup, Item No. NBCA-12M-W 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… and 15 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Initiation date Oct 20, 2015
Report date Nov 25, 2015
Termination date Nov 9, 2016
City San Diego
State CA
Country United States
FEI number 3003789989

At a glance

  • 10–99 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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