Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of QIAGENLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list QIAGEN Gaithersburg, Inc. with 2 device recalls. The most recent is a device recall dated Jan 30, 2013: QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Product Usage: The artus ….
| Jan 30, 2013 | QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Product Usage: The artus CMV RG PCR ASR is designed to detect and to quantifClass II · CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials. | Device recalls |
| Jan 30, 2013 | QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Product Usage: Test is intended for use in the detection and quantitation of Class II · CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials. | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built