Health & Personal Care Recalls

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.

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Lack of Assurance of Sterility

GM Gumili Wintergreen Essential Oil Recalled for Child Poisoning Risk

Organic Zing Birch Essential Oil Recalled Over Child Poisoning Risk

Fresenius Kabi Compounding Recalls Acyclovir Sodium Injection Due to Sterility Risks

Lack of Assurance of Sterility

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.

Remel Recalls Campy CVA Medium Over Low Recovery Rates

Remel, Inc. recalled 97 units of Campy CVA Medium on February 5, 2026. Customers reported low to no recovery of Campylobacter Jejuni ATCC 33291 in the affected lot. Healthcare providers and patients must stop using the product immediately.

Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Packaging (2026)

Diagnostica Stago STA Liatest Free Protein S Kit Recalled for 369 Units Worldwide in 2026

The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.

GE Medical Systems Recalled 125 Imactis CT-Navigation System Stereotaxic Accessories in 2026

There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.

Exactech Equinoxe Ergo 321-09-05 Impactor Handle Recall (120 Units, 2026)

Impactor handle may be missing cross-pin

Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)

Exactech Equinoxe Core Instrument Kit KIT-311X Recalled for Missing Cross-Pin

Impactor handle may be missing cross-pin

B. Braun Medical Recalls BBraun Medical 21G Winged INF 7B3050 for 105,550 Units (2026)

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

B. Braun Medical 21GA Winged Infusion Set 7M2802 Recalled 51,300 Units (2026)

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.