immediate action Recalls

SunMed Recalls Broselow Pediatric Emergency Tape Over Dosing Errors

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

ICU Medical Recalls Plum Duo Infusion Pump Over High Hazard Risk

ICU Medical recalled the Plum Duo Infusion Pump on December 15, 2025, after reports of malfunctioning flush programming. The recall affects models 400020401 and 400021001 sold worldwide. This issue may pose a high risk to patient safety.

Philips Medical Systems Recalling Allura Xper FD10 Over Electrical Risk

LEASEIR Surgical Laser Recalled Over Missing Danger Label

The console label for affected devices is missing the "DANGER" symbol.

Intuitive Surgical Recalls da Vinci SP Access Port Kits Over Sterility Risk

Access Port System tray may develop cracks potentially resulting in a sterility breach.

So Delicious Dairy Free Frozen Dessert Recalled Due to Foreign Material

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.

Broselow Recall Due to Dangerous Dosing Errors in ALS Organizer

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

ICU Medical Recalls Plum Duo IV Pump Due to High Hazard

Philips Medical Systems Recalls Allura Xper FD20 Over Electrical Hazard

Sysmex America Recalls Tube Sorter Due to Lift Hazard

Sysmex America recalled 44 units of the TS-10/TS-10H Tube Sorter on December 15, 2025. The electromagnetic holding force may disengage, causing unintended movement. Healthcare providers should stop using the device immediately.

Philips Medical System Recall Over Electrical Hazard Risk

Immunotech A.S. Recalls Estrone RIA Kit Over False Results Hazard

Immunotech A.S. recalled 160 Estrone RIA kits on December 15, 2025, due to a risk of falsely high patient results. This class II recall affects kits distributed in multiple countries, including the US and several European nations.

Philips Medical Systems Recalls Allura Xper FD10 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.

ICU Medical IV Pump Recalled Due to Programming Error Risk

D. Coluccio & Sons Recalls Amaretti Cookies Over Poison Risk

D. Coluccio & Sons recalled 800 units of Sapori Amaretti Almonds cookies on December 14, 2025, due to elevated hydrocyanic acid levels. The cookies were distributed in New York, New Jersey, Georgia, and California.

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 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.

Prima Vera Nueva Recalls Butternut Squash Tamales for Listeria Risk

Potential contamination with biological hazards (Listeria monocytogenes).