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

Recall Z-1815-2012 — PrepStain GN 480 Disposable Kit Catalog/Model 490542 This is a complete kit, per the firm's explanation, that contains the PrepStain Syringing Pipettes 240, the product being recalled. The affected lots are listed under those pipettes (PrepStain Syringing Pipettes 240)

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-1815-2012
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.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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.

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