Health & Personal Care Recalls

Philips Medical System Recall Over Electrical Hazard Risk

Philips Recalls Allura Xper FD20 Over Electrical Hazard

Philips recalled 79 Allura Xper FD20 systems on December 15, 2025. The recall affects systems with an improperly installed drip tray which can cause electrical short-circuits. Healthcare providers and patients must stop using the device immediately.

Philips Medical Systems Recalls Allura Xper FD20/20 Over Electrical Hazard

Philips Medical Systems Recalls Allura Xper FD20 Biplane Over Electrical Hazard

Philips Medical Systems recalled 23 units of the Allura Xper FD20 Biplane on December 15, 2025. The recall affects systems with improperly installed drip trays, posing an electrical hazard. Health providers and patients must stop using the device immediately.

Philips Recalls Allura Xper FD20 OR Table Due to Electrical Hazard

Philips Medical Systems Recalls Allura Xper FD10 Over Electrical Hazard

Wilson-Cook Medical Recalls Nasal Jejunal Feeding Tube Over Missing Component

Wilson-Cook Medical recalled 60 units of Nasal Jejunal Feeding Tube NJFT-10 on December 15, 2025. The tubes were packaged without the necessary nasal transfer tube component. This defect poses a high hazard risk for patients requiring feeding assistance.

Philips Recalls Allura Xper FD20 Biplane Over Electrical Hazard

ICU Medical Recalls Plum Duo Infusion System Over Speaker Failure

ICU Medical recalled 423 units of the Plum Duo Infusion System on December 15, 2025. Defective primary speakers may fail to produce audible alarms and alerts. This poses a high hazard risk to patients reliant on the device for medication administration.

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 Kits Recalled Due to Cracked Tubing 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 Medical Kits Recalled Over Hazardous Adhesive

Medline Industries recalled 236 medical procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive that may cause butyrate tubing to crack. Patients and healthcare providers should stop using these kits immediately.

Medline Medical Kits Recalled Due to Liquid Adhesive Hazard

Medline Industries, LP recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive linked to cracking tubing during use. Healthcare providers and patients must stop using these kits immediately.

Medline Convenience Kits Recalled Over Adhesive Hazard

Medline Industries recalled select medical procedure convenience kits on December 12, 2025. The recall affects 40 units due to risks associated with MASTISOL liquid adhesive. The adhesive's tubing may crack during use, posing safety concerns.

Medline Recalls Medical Kits Over Adhesive Tubing 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 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 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 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.

Philips Azurion System Recalled Due to Software Malfunction

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.