Class IIOngoingZ-1854-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode
Potential for detachment of a distal tip component of the device during use.
Olympus Corporation of…PAApr 29, 2026
Class II recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 697–708 of 3,866 recalls
Class IIOngoingZ-1853-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode
Potential for detachment of a distal tip component of the device during use.
Olympus Corporation of…PAApr 29, 2026
Class IIOngoingZ-1852-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode
Potential for detachment of a distal tip component of the device during use.
Olympus Corporation of…PAApr 29, 2026
Class IIOngoingZ-1851-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode
Potential for detachment of a distal tip component of the device during use.
Olympus Corporation of…PAApr 29, 2026
Class IIOngoingZ-1850-2026
Medline Industries, LP recalls Medline Kits: 1) ARTHROSCOPY PACK
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1849-2026
Medline Industries, LP recalls Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1848-2026
Medline Industries, LP recalls Medline Kits: 1) D AND C PACK
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1847-2026
Medline Industries, LP recalls Medline Kits: 1) HYSTEROSCOPY PACK
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1846-2026
Medline Industries, LP recalls Medline Kits: 1) GYN LAPAROSCOPY PACK
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1845-2026
Medline Industries, LP recalls Medline Kits: 1) LABOR PACK-22025208-LF
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1844-2026
Medline Industries, LP recalls Medline Kits: 1) ARTHROGRAM TRAY
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026
Class IIOngoingZ-1843-2026
Medline Industries, LP recalls Medline Kits: 1) SYR CONTROL 8ML ROTATING
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LPILApr 29, 2026