burn risk Recalls

GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)

Frontier Devices 301.914S2 14 mm Distraction Pin Recalled for Unvalidated Shelf Life (High Risk)

Labeling includes shelf life that has not been validated.

IBC Technologies CX Series Combi Boilers Recalled for Burn Hazard (2025)

Abbott i-STAT CG4+ Cartridge Recall: 9,067,050 Units Across U.S. With 510(k) Clearance Issue (2025)

Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.

Boston Scientific Pacemaker L231 Recalled; 63,851 Units in 2025

Boston Scientific ESSENTIO DR EL MRI Pacemaker Recalled for Software Safety Issue (190,088 Units, 0)

Boston Scientific Pacemakers Recall 28,911 U128 ACCOLADE, VISIONIST VALITUDE CRT-P Devices (2025)

B. Braun Sodium Chloride Injection 1000 mL Recalled nationwide for particulates (Class I)

B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.

Synergy Housewares Recalls Wolfgang Puck Petite Tea Kettles for Burn Hazard (14 oz) Sold on HSN

Empower Brands Recalls Remington Hair Dryers Over Electrocution Hazard (2025)

Firefly Safe & Green 32 oz. Fuel Bottles Recalled for Poisoning Risk to Children

ESR HaloLock Wireless Power Banks Recalled for Fire Hazard (3 Models) 2025

ESR HaloLock wireless power banks, distributed by Waymeet, are recalled. The lithium-ion battery can overheat and ignite, creating a fire and burn hazard. Stop using the recalled power banks and contact Waymeet for a full refund.

Fresh & Ready Foods Tuscan Artichoke and Mozzarella Salad Recalled for Undeclared Allergens (8.5 oz)

undeclared allergen (Wheat and Milk) on ready to eat sandwiches.

Philips CT Systems Recalled for Descent Hazard In 210-Unit Worldwide Distribution (2025)

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Beckman Coulter DxH 900 COULTER Hematology Analyzer Recalled for Inaccurate Hemoglobin Results

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier (UDI) in 206 Units

The device does not bear a unique device identifier.

Max Mobility/Permobil Recalls 8,413 Smart Drive MX2+ SpeedControl Dials (2025)

Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.

Domino Foods Recalls 4,500 Bags of Pure Cane Granulated Sugar Over Contamination Risk (2025)

Domino Foods recalled 4,500 bags of Pure Cane Granulated Sugar distributed in California and Utah. The sugar may contain foreign objects. Consumers should stop using it and contact Domino Foods for refund or replacement.

SUNGAL UDK Half Plum 170 g Recall for Cyclamate Adulteration (2025)

Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units

Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.