burn risk Recalls

URMYWO Baby Loungers Recalled for Suffocation and Fall Hazards; 2025 Recall Active

Philips Allura Xper FD20 Recall Affects 2,114 Units Globally Over Power Component Deterioration

Philips Medical Systems Nederland B.V. Allura CV20 Recalled in Global Distribution for Component D-7

Philips Allura Xper FD10 Recalled for BIOS Battery Startup Failure (2,317 Units Worldwide, 2025)

Philips Medical Systems Nederland Recall: BIOS Battery Causes Startup Failures in Allura Xper CV20 7

New Spirit Naturals Gluta Plus Glutathione 60-Capsule Recall for Milk Allergy Hazard

BigTree Sales Recalls BT-GERMWAND-LRG-WHT UV-C Wand for Unsafe Radiation Risk (2025)

ImaCor ClariTEE Miniaturized TEE Probe CLT-010 Recalled Over Reversed Articulation Risk (2025)

Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.

Getinge 88-Series Washer-Disinfector 88-5 Recalled for Overheat Risk in 788 Units (2025)

Potential for device to overheat during operation f the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.

Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

Northeast Scientific NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter Recall 2025

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

Air Vent Attic Fan Motors Recalled for Fire Hazard in 2003-2013 Models (2025)

Party Favors Lite-Up Torches and Laser Pointers Recalled for Battery Ingestion Risk

Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.

Siemens MAGNETOM Cima.X MRI Recall: 9 Units Worldwide (2025)

Middlefield Original Cheese Cooperative Recalls 7,455 lbs Shredded Mozzarella/Provolone (5-lb Bags)

Potential contamination with Listeria monocytogenes

Chlorpromazine Hydrochloride Tablets Recalled Over Foreign Substance Found in Packaging Coil (High-R

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

One lot manufactured with an invalid sterilization cycle.

Ultra Violette Mini Mates SPF 50 Kit Recalled for SPF Variability in 44,497 Tubes (2025)

Ultra Violette Mini Mates SPF 50 kit sold nationwide in the U.S. is recalled. Testing showed SPF results ranging from 4 to 64. The recall is issued by Grace & Fire USA Inc. The public was notified by letter.

CooperVision MyDay Toric Contact Lenses Recalled for Invalid Sterilization Cycle

CooperVision recalled 4,140 MyDay Toric contact lenses sold nationwide in the United States. The recall cites an invalid sterilization cycle for one lot. Patients should stop wearing the lenses and consult their eye care providers for guidance.

Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected

Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.