Health & Personal Care Recalls

Fujirebio Diagnostics Recalled pTau 217 Plasma Cartridges

Applied Medical Resources Recalls Cannula Due to Blade Hazard

There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.

Instrumentation Laboratory Recalls Coagulation Testing Device Due to Contamination Risk

Instrumentation Laboratory recalled 7,720 coagulation testing devices on December 11, 2025. The recall stems from a potential for microbial contamination. Healthcare providers and patients should stop using the device immediately.

Fujirebio Diagnostics Recalls Plasma Calibrators Over Inaccurate Results

Fujirebio Diagnostics Recalls Diagnostic Test Over Inaccurate Results

Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Calibrators

Fujirebio Diagnostics Issues Recall for Inaccurate Test Results

Fujirebio Diagnostics Recalls Lumipulse ¿-Amyloid Controls Over Test Inaccuracy

Mazor Robotics Recalls Robotic Guidance System Over Software Errors

Software errors that can result in incorrect surgical instrument positioning during spinal surgery.

Elekta Recalls MOSAIQ Oncology System Over Overtreatment Risk

Elekta recalled the MOSAIQ Oncology Information System on December 10, 2025. A malfunction may cause overtreatment in patients due to software issues. Healthcare providers should stop using the device immediately and follow recall instructions.

GE HealthCare Recalls Nuclear Medicine Systems Over Fall Risk

GE HealthCare recalled three Nuclear Medicine systems on December 10, 2025. The recall follows concerns over inadequate detector support, which could lead to a fall and serious injury. No incidents have been reported to date.

REPLIGEN Spectrometer Recalled Due to Laser Hazard

REPLIGEN Corporation recalled 33 Maverick Measurement Module Spectrometers on December 10, 2025. Disconnected or poorly crimped cables may cause elevated laser output or unintended firing. The recall affects devices distributed in the U.S.

GE HealthCare Recalls Nuclear Medicine Systems Over Fall Risk

GE Healthcare Recalls Nuclear Medicine Systems Due to Fall Hazard

GE Healthcare recalled seven Nuclear Medicine systems on December 10, 2025, due to potential detector falls. The recall affects systems that have exceeded their End of Guaranteed Service. No injuries or falls have been reported.

GE HealthCare Recalls Nuclear Medicine Systems Due to Fall Risk

Intuitive Surgical Recalls 2,095 da Vinci S, Si EndoWrist Tenaculum Forceps Instrument (2025)

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Intuitive Surgical da Vinci S, Si Grasping Retractor Instrument Recalled for 2,660 Units (2026)

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Intuitive Surgical recalls 2,370 da Vinci S/Si Double Fenestrated Grasper Instruments (2026)

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Intuitive Surgical da Vinci S/Si EndoWrist Recall 6,152 Instruments for Pitch Cable Frays (2026)

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Intuitive Surgical da Vinci S/Si Monopolar Curved Scissors Recall for 86,904 Units Worldwide (2025)

Due to increased complaints for broken/frayed grip cables for reusable instruments.