Product Wiki · Recalls · U.S. FDA — Device Enforcement

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 configurations of these Drugs of Abuse Tests consist of a combination of drug strips, including Benzodiazepine — recall Z-0299-2016

U.S. FDA — Device Enforcement · United States · 2015-10-20 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0299-2016
Date of alert: 2015-10-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Ameditech Inc
Product category: device
Product type: Devices

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

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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