Every recall we track for Guangzhou Pluslife Biotech Co., Ltd. — 2 in all — plus the complaints and injury reports the public filed about them.
Guangzhou Plus: MiniDock Integrated Nucleic Acid Testing Device (PM001) recalled due to lack of FDA premarket authorization. No remedy specified in official notice.
Pluslife SARS-CoV-2 Nucleic Acid Testing Cards (model RM1010202) were distributed without FDA premarket authorization. Consumers should check if they have these kits and contact the manufacturer for details.
