Devices

Device Recall DrugCheck Drugs of Abuse Ketamine Dip Test

Model / Serial
PC 09077, PC03227, PC03055, PC09293, PC11115, PC08126, PC06276, PC07085, PC06305, and PC08017.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide Distribution -- US, including the states of CA, NY, MN, and SC; SWEDEN, CANADA, UNITED KINGDOM, and GUATEMALA.
Product Description
DrugCheck Ketamine Dip Test || 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT. || This assay provides only a preliminary analytical test result.
Manufacturer
Express Diagnostics Int'l., Inc.
1 Event
- Recall of Device Recall DrugCheck Drugs of Abuse Ketamine Dip Test

Manufacturer

Express Diagnostics Int'l., Inc.

Manufacturer Address
Express Diagnostics Int'l., Inc., 1550 Industrial Dr, Blue Earth MN 56013-1100
Manufacturer Parent Company (2017)
Express Diagnostics Intl Inc.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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