Z-0569-2026 Class II Ongoing
FDA device recall Z-0569-2026 was initiated by Meridian Bioscience Inc on October 7, 2025 and is designated Class II. Reason for recall: The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume. The recall status is ongoing. Affected quantity: 109 in total.
Recall Details
- Product Type
- Devices
- Report Date
- November 26, 2025
- Initiation Date
- October 7, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 109 in total
Product Description
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay
Reason for Recall
The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.
Distribution Pattern
US Distribution to states of: AL, CO, FL, GA, IL, MD, ME, MT, NH, NJ, OH, TN, TX and WA; and OUS (foreign) countries of: Canada, Italy, and Panama.
Code Information
UDI/DI 00840733102196, Lot Numbers: 480350U020, Exp. 2026-06-12