chemical hazard Recalls

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

Augmentation devices failed bacterial endotoxin testing.

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.

Valley Springs Bottled Water Recalled Over Insanitary Conditions

Water was bottled under insanitary conditions.

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Lack of Assurance of Sterility

GM Gumili Wintergreen Essential Oil Recalled for 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.

EnHomee 10-Drawer Dressers Recalled for Tip-Over Hazard (2026)

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

IF Holding II Tippy Toes Baby Food Recalled for Patulin Contamination (2026) 1,375 cases

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.

Pure Solutions Recalls Sleep Formula Over Milk Allergen Risk

Pure Solutions recalled 442 bottles of its sleep supplements on February 3, 2026. The labels did not declare a milk allergen despite containing bovine colostrum. Consumers should stop using the product immediately and seek refunds.

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

Impactor handle may be missing cross-pin

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Deviations

Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.