Class I Recall of QIAGEN Filter Tips

Published: 08/05/2019

  • Food and Drug Administration
Relevant To:
  • All Healthcare Organizations

The U.S. Food and Drug Administration (FDA) has announced a Class I recall of QIAGEN filter tips for use with the QIAsymphony SP/AS instruments due to potential to leak, which may result in delayed or inaccurate results. Customers have reported splashes on the QIAsymphony instrument, liquid in the tip guard, dripping/leaking tips, failed test signals, empty wells indicative of volume loss, and incorrect test results with use of the defective tips.

Severe adverse health consequences, including

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