immediate action Recalls

Merck Emend Recalled Due to Potential Metal Contamination

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

Prima Vera Nueva Tamales Recalled for Listeria Risk

Prima Vera Nueva recalled 9,656 packages of Roasted Pumpkin & White Cheddar Tamales on December 12, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not eat these tamales and seek refunds immediately.

Prima Vera Nueva Tamales Recalled Over Listeria Contamination

Potential contamination with biological hazards (Listeria monocytogenes).

Prima Vera Nueva Tamales Recalled Due to Listeria Risk

Prima Vera Nueva recalled 16,264 packages of Mushroom, Spinach & Salsa Tamales on December 12, 2025. The recall stems from potential contamination with Listeria monocytogenes, a serious foodborne illness. Consumers should not eat the product and seek a refund.

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.

Prima Vera Nueva Recalls Tamales Due to Listeria Risk

Prima Vera Nueva recalled 30,327 packages of Butternut Squash Tamales on December 12, 2025. The product poses a high risk of contamination with Listeria monocytogenes. Consumers should not consume these tamales and should seek a refund or replacement.

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.

1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6

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.

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.

Integra LifeSciences Recalls ICP Sensor 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.

Philips Recalls Patient Monitors Over Connectivity Issue

It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.

2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8

Philips Azurion System Recalled Due to Software Malfunction

Merck Recalls Noxafil Oral Suspension Due to Metal Contamination

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

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.

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 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.

Prima Vera Nueva Tamales Recalled Due to Listeria Risk

Potential contamination with biological hazards (Listeria monocytogenes).

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.