Drug Recalls Center

Broselow Recall Due to Dangerous Dosing Errors in ALS Organizer

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.

Elekta Recalls Medical Linear Accelerators Due to Grounding Issues

Elekta recalled 5,391 medical linear accelerators on December 14, 2025. A manufacturing issue related to electrical grounding poses a serious hazard. Patients and healthcare providers must stop using these devices immediately.

Medline Medical Procedure Kits Recalled Due to Tubing Hazard

Medline recalled 96 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that can crack during use. Patients and healthcare providers should stop using these products immediately.

Medline Medical Kits Recalled Over Adhesive Tubing Risk

Medline Industries recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which has defective butyrate tubing. Cracking during use poses a high risk to patients and healthcare providers.

Medline Medical Kits Recalled Due to Hazardous Adhesive

Medline Industries recalled 1,928 medical procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective butyrate tubing. Patients and healthcare providers must stop using these kits immediately.

Philips Azurion System Recalled Due to Software Malfunction

Elekta Recalls Leksell GammaPlan Software Due to High Radiation Risks

Medline Medical Procedure Kits Recalled Over Adhesive Hazard

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

Medline Recalls Medical Kits Due to Adhesive Tubing Hazard

Medline Industries recalled 117 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that may crack. Stop using these kits immediately and follow manufacturer instructions for return.

Medline Medical Kits Recalled Over Tubing Cracking Hazard

Medline Industries recalled 60 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive which has a defect causing butyrate tubing to crack. Users must stop using the kits immediately and follow recall instructions.

Medline Recalls Nerve Block Tray Kits Over Cracked Tubing Risk

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

MediNatura Recalls ClearLife Allergy Nasal Spray for Contamination

MediNatura recalled ClearLife Allergy Nasal Spray on December 12, 2025, due to microbial contamination. The product contains yeast, mold, and Achromobacter. Consumers should stop use immediately and contact healthcare providers.

Bard Peripheral Vascular Recalls CV Catheter Due to Sterility Risk

Due to damage to outer tray that can potentially compromise the sterile barrier

Merck Emend Recalled Due to Potential Metal Contamination

Presence of particulate matter: potential presence of metal particulates in the product.

MediNatura Recalls ReBoost Nasal Spray Due to Microbial Contamination

MediNatura recalled ReBoost Nasal Spray on December 12, 2025, due to microbial contamination. The affected product, distributed nationwide, contains yeast/mold and Achromobacter. Consumers should stop using the product immediately.

Philips Recalls Azurion Systems Over Software Issues

Philips recalled 10,466 Azurion Systems on December 12, 2025, due to six software issues that can cause system failures. Users must stop using the devices immediately. The recall affects models sold worldwide, including in the U.S.

Hologic Recalls ThinPrep CytoLyt Solution Due to Fungal Contamination

Hologic, Inc. recalled 3,728 units of ThinPrep CytoLyt Solution on December 12, 2025. The recall follows the discovery of fungal contamination with Parengyodontium album. Patients and healthcare providers must stop using the affected products immediately.

Merck Recalls Noxafil Oral Suspension Due to Metal Contamination

Presence of particulate matter: potential presence of metal particulates in the product.

Medline Medical Kits Recalled Due to Hazardous Adhesive

Medline recalled multiple medical procedure convenience kits on December 12, 2025. The recall affects 66 units containing MASTISOL liquid adhesive. The adhesive's tubing may crack, posing a serious risk during use.

Elekta Recalls Radionuclide RT Treatment Planning System Over High-Risk Error

Elekta recalled the Leksell GammaPlan RT Treatment Planning System on December 12, 2025, due to a software error. This defect may lead to incorrect patient irradiation if not detected. Healthcare providers must stop using the software immediately.

NIPRO Technical Services Recalls Conductivity Solutions Over Calibration Risk

due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.

Medline Medical Kits Recalled Due to Adhesive Hazard

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

Medline Circumcision Kits Recalled Over Adhesive Hazard

Medline Industries, LP recalled 1,928 circumcision procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which may crack during use. Healthcare providers and patients must stop using these kits immediately.

Integra LifeSciences Recalls Codman Microsensor Kit Over Corrosion Risk

Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.