Guangzhou Pluslife Biotech Co., Ltd.
Guangzhou Pluslife Biotech Co., Ltd. appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1978-2025, Class II) was initiated on January 24, 2025.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1978-2025 | Class II | Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PM | January 24, 2025 |
| Z-1979-2025 | Class II | Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Cata | January 24, 2025 |