Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/a
Recall
- Recall Number
- Z-1504-2025
- Event Number
- 96521
- Firm
- Qiagen Sciences LLC
- FEI Number
- 3003572099
- Product Code
- QOF
- Status
- Open, Classified
- Root Cause
- Mixed-up of materials/components
- Initiated
- March 12, 2025
- Posted
- March 31, 2025
- Address
- 19300 Germantown Rd, Germantown, MD, 20874-1415
Description
Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/a
Identified faulty cartridges. If such a faulty cartridge is used for sample testing, false test results could occur.
On March 12, 2025, "URGENT MEDICAL DEVICE CORRECTION" letters were sent to customers. Actions to be taken by customer/user: 1. Check if you have remaining stock. DO NOT use it. Dispose of it immediately in accordance with your national and local safety and environmental regulations. 2. Contact QIAGEN Technical Services for a free-of-charge replacement. o If you already used cartridges from this LOT, identify the results obtained with cartridges from the affected SN. For results obtained with an affected SN: Review all results of the respective targets mentioned in Detailed description of the issue, above, to identify potentially erroneous diagnosis, except in those cases where alternative confirmation was obtained. o Review any result for which tests were performed, or treatments were given on clinical and/or epidemiological suspicion of the respective targets. 3. Review this notice with your laboratory/medical director. 4. Important: Forward this information to all individuals and departments within your organization using the above-listed kits. If you are not the end user, forward this notice to the product end user. 5. Complete the Acknowledgement of Receipt Form Actions taken by QIAGEN: QIAGEN was able to identify the root cause of the issue and has implemented immediate actions to ensure that the currently produced cartridges will not cause this issue moving forward. If you have any questions or concerns, please contact your local QIAGEN Technical Services Department through any of the following: Telephone: 800 362 7737; Email: [email protected]
US Distribution: AL, CA, DC, FL, IN, KS, KY, MA, ME, MN, NY, and TX.
445 units