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.
205 recalls tagged with “laceration risk”.
undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
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.
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology recalled 1,780 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. Distal tips on these devices may detach at lower than expected forces. Stop using immediately and follow the recall instructions.

Enoxaparin Sodium Injection recall active as of 2025. Cardinal Health and Sandoz Inc. distributed the product in Kansas. Bags labeled 80 mg/0.8 mL contained 30 mg/0.3 mL doses. Health authorities urge immediate stop-use and guidance from providers.
Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is labelled Cool Mint/Whitening. The toothpaste inside the tube is Fresh Mint as indicated on the outer carton
Contains undeclared wheat. The top label identifies the product as potato salad, but the unit contains pasta salad.
Lack of Assurance of Sterility.




Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.
Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.

Potential contamination with Listeria monocytogenes
DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.