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

Recall Z-2088-2019 — Filter-Tips, 1500 ul (1024 tips/kitbox), REF 997024- REF: 997024 IVD: Used with the QIAGEN QIAsymphony SP/AS Instruments (REF 9001297 and 9001301) REF: 997024 Used in sample preparation

U.S. FDA — Device Enforcement · United States · 2019-06-05 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2088-2019
Date of alert
2019-06-05
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Qiagen Sciences LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0605020019
Reported risk: Kit lots contain a small percentage of damaged Filter-Tips that are leaking when being used with the QIAsymphony SP/AS Instruments (REF 9001297 and 9001301)
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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