stop use immediately Recalls

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.

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

Augmentation devices failed bacterial endotoxin testing.

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.

Dresbe LED Christmas Headbands Recalled Over Battery Ingestion Risk (2026)

Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Lack of Assurance of Sterility

Semfri Children's Helmets Recalled Over Serious Head Injury Risk

Semfri recalled children's helmets on February 5, 2026, due to safety violations. The helmets do not comply with mandatory safety standards, posing a serious risk of head injury. Consumers should stop using the helmets immediately and seek a refund.

GM Gumili Wintergreen Essential Oil Recalled for Child Poisoning Risk

Lola Plus The Boys Recalls 5 Youth Hoodies With Drawstrings Over Strangulation Risk (2026)

Little Cow Company Recalls 9 oz Glass Jar Candles Over Fire, Burn and Laceration Hazards (2026)

Aterian Recalls PurSteam Elite Travel Steamers and Mighty Lil Steamers for Burn Hazard (2026)

Kitosun Submersible LED Lights Recalled Over Battery Ingestion Risk

Organic Zing Birch Essential Oil Recalled Over Child Poisoning Risk

Fresenius Kabi Compounding Issues Recall of Vancomycin Injection

Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.

Fresenius Kabi Compounding Recalls Ketamine Injection for Sterility Risk

Fresenius Kabi Compounding recalled 1,410 bags of ketamine HCl injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers and consumers must stop using this product immediately.

Fresenius Kabi Compounding Recalls Thiamine Injection Over Sterility Risk

Fresenius Kabi Compounding recalled 10,548 bags of thiamine HCl injection on February 5, 2026. The recall follows a lack of assurance of sterility, posing a high health risk. Affected products include several lots expiring between February and May 2026.