Z-1164-2025 Class II Ongoing
FDA device recall Z-1164-2025 was initiated by Microbiologics Inc on January 20, 2025 and is designated Class II. Reason for recall: Internal quality control procedures were not followed correctly for the testing/release of three lots of 8234/8235. This resulted in the release of products that should have failed and been discarded.… The recall status is ongoing. Affected quantity: 27 units.
Recall Details
- Product Type
- Devices
- Report Date
- February 19, 2025
- Initiation Date
- January 20, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 27 units
Product Description
Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel (Inactivated Pellet), REF 8235; in-vitro diagnostic test
Reason for Recall
Internal quality control procedures were not followed correctly for the testing/release of three lots of 8234/8235. This resulted in the release of products that should have failed and been discarded. The concentration of one target (HPV 16 L1) was low enough to cause QC failures, no detection, or invalid results on some instruments and assays.
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Netherlands, Sweden, UK, France, Australia, New Zealand.
Code Information
UDI/DI 70845357043077, Lot Numbers: 8235-32, 8235-33