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

PrepStain Installation Kit (PreCoat), Catalog/Model # 490528 — recall Z-1813-2012

U.S. FDA — Device Enforcement · United States · 2012-03-22 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1813-2012
Date of alert
2012-03-22
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Tripath Imaging, Inc.
Product category
device
Product type
Devices
Reported risk: The PrepStain Syringing Pipettes may not dispense the minimum volume of 7.5 mL of the sample due to leaking. This event resulted in an increase in complaints of leaking syringing pipettes
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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