
FDA•CRITICAL
D'Dioses Fruit Pops: multiple undeclared allergens
32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
32 products
32 D'Dioses Fruit Pops products recalled for undeclared tree nuts or milk.
32 products
Argon Medical recalls pacing electrode trays over non-sterile lidocaine ampules.
6 products
Abiomed recalls Impella RP Flex pump sets over introducer sheath leakage risk.
13 products
BMW is recalling certain 530e, 740Le, and 330e iPerformance vehicles due to an engine starter relay that may corrode and cause a fire.

Ohm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.

Trafa Pharmaceuticals is recalling 15 kg bags of Organic Moringa Leaf Powder due to potential Salmonella contamination.

Fusia Kimchi & Tofu Kimbap recalled due to undeclared fish allergen.

Medline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.

Medtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.

Kia is recalling 2020-2024 Telluride vehicles due to a risk of fire from overheating front power seat motors.

Hyundai is recalling 2023-2024 Ioniq 5 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.

Kia is recalling 2022-2024 EV6 and 2024 EV9 vehicles due to a high voltage battery defect that may cause a fire while parked or driving.

Crestline is recalling 2026 Ford CCL166 Type III emergency vehicles due to a fuel line puncture risk that may cause a fire.

Windstone Medical recalls DSAEK Pack-RX kits due to contaminated alcohol prep pads.
4 products
Baxter recalls Hillrom VOLARA P.CIRCUIT KIT (REF M08085) over nebulizer cup leakage that may cause oxygen drop and ineffective treatment.
4 products
Spring & Mulberry is recalling Mango Chili and Pecan Date-Sweetened Chocolate bars due to potential Salmonella contamination.
11 products
Hamilton Medical is recalling ventilator coaxial breathing circuits due to a risk of valve membrane adhesion and inadequate ventilation.
