Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 4081–4100 of 39,430 recalls
Guangzhou Pluslife Biotech Co., Ltd.
Devices were distributed in the U.S. market without obtaining the required FDA premarket authorization (e.g., 510(k) clearance or PMA).
Guangzhou Pluslife Biotech Co., Ltd.
Devices were distributed in the U.S. market without obtaining the required FDA premarket authorization (e.g., 510(k) clearance or PMA).