High Risk Recalls

Boston Scientific EndoVive PEG Kit Recalled for Sterility Risk in 806 Kits (2026)

LEO Pharma Recalls Adbry Injection Over Sterility Concerns

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.

VERGANI 1944 MILANO Pandoro Classico Gluten Free Recalled by Italianway Import (60 Units)

Potential contamination with foreign material (Teflon fragments) from flaking cooking molds.

SLADE GORTON Recalls Salmon Over Listeria Contamination

SLADE GORTON & CO. recalled 190 cases of Wellsley Farms Atlantic Salmon on February 10, 2026. The product may contain Listeria monocytogenes, a serious health risk. Consumers should not consume this product and seek a refund or replacement.

Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)

Hortex Mieszanka 9 Recall for Glass Contamination in 2026

Airova Recalls Aroeve Air Purifiers Due to Fire Hazards

H & N Group Recalls Frozen Shrimp Over Cesium-137 Risk

H & N Group recalled 378 cases of frozen cooked shrimp on February 9, 2026. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume the shrimp and seek refunds.

BD Kiestra ReadA Lab Automation Module Recalled in 2026 Over Connectivity Delays (82 Units)

12 Million TRUE METRIX Blood Glucose Meters Recalled Due to E-5 Error Code Risk

Trividia Health TRUE METRIX PRO Owner's Booklet Recall for 1,001,534 Units (2026)

International Life Sciences Recalls Artelon FLEXBAND TWIST Augmentation Devices for Endotoxin Test F

Augmentation devices failed bacterial endotoxin testing.

Trividia Health TRUE METRIX GO Recall for E-5 Error Misleading Labeling (1.4M, 2026)

Trividia Health Recalled 3.68 Million TRUE METRIX AIR Booklets for E-5 Error (2026)

International Life Sciences Recalls Artelon FlexBand Dynamic Matrix 31057 for Endotoxin Testing Fail

Augmentation devices failed bacterial endotoxin testing.

Valley Springs Distilled Water Recalled Over Insanitary Conditions

Valley Springs Artesian Gold recalled 263,440 gallons of distilled water on February 6, 2026. The water was bottled under insanitary conditions, posing a health risk. Consumers in Illinois and Wisconsin should not consume the affected products.

International Life Sciences Recalls Artelon FlexBand Plus Augmentation Devices for Endotoxin Testing

Augmentation devices failed bacterial endotoxin testing.

Valley Springs Bottled Water Recalled Due to Insanitary Conditions

Valley Springs recalled 379,868 units of bottled water on February 6, 2026. The recall affects multiple sizes and brands due to insanitary bottling conditions. Consumers should not consume the product and seek refunds or replacements.

Hitachi Proton Beam Therapy Device Recalled for Software Issues

Hitachi Ltd. recalled one unit of its Proton Beam Therapy System on February 6, 2026 due to a software anomaly. The issue may result in positional discrepancies during patient treatment. The recall affects distribution in Texas and Washington D.C.

Hitachi Proton Beam Therapy System Recalled Due to Software Issue

Software anomaly in the patient positioning system may result in positional discrepancy.