
burn risk Recalls
471 recalls tagged with “burn risk”.


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.
Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard
Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage
Heraeus Medical GmbH recalled PALACOS R pro 40 and R pro 80 bone cement on December 9, 2025. The recall follows multiple complaints of ampoule breakage affecting product usability. Healthcare providers must stop using the product immediately.
Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard
Heraeus Medical GmbH recalled PALACOS MV pro 40 and MV pro 80 bone cement on December 9, 2025. The recall follows numerous complaints about ampoule breakage. This defect can prevent proper cement dough formation, rendering the product unusable for patients.
Heraeus Medical Recalls PALACOS Bone Cement Due to Breakage Risk
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.

Siemens Recalls LUMINOS Medical Imaging Systems Over Collimation Risk

Cubimana Tree House Building Toy Sets Recalled for Battery Ingestion Risk Sold on Shein by Vatos T o
Merit Medical Recalls Vascular Tray Over Detaching Handle Hazard
Inflation device handle may detach from the syringe during procedure.

Primark Water Balloon Pumps Recall 5252801 Over Rupture Hazard (2025)
This recall involves Primark Water Balloon Pumps, which were sold in blue and pink. The pumps are shaped like a water bottle with a spray head. The product code 5252801 is printed on the price tag located on the back of the water balloon pump bottle.
Merit Medical Recalls Custom Procedure Kits Due to Detachment Hazard
Inflation device handle may detach from the syringe during procedure.
Zimmer Recalls Affixus Femoral Nails Over Fatigue Fracture Risk
Zimmer, Inc. recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. These implants may have an undersized distal diameter that could lead to fatigue fractures. Patients should stop using the device immediately and contact their healthcare provider.