State
72,940 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.
Of the 385 recalls naming Guam we have scored against our rubric, 14 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 37 (10%) are Severe.
Which agencies issued them
These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Imprimis NJOF is recalling 778 boxes containing 15,540 pre-filled syringes of Dexamethasone and Moxifloxacin intraocular injection over glass-like particles.
Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.
Ziyad Brothers Importing is recalling 575 cases of Baraka Gourmet Pastry Kunafe because the product may contain partially hydrogenated oils.
Alembic Pharmaceuticals is recalling Fesoterodine Fumarate Extended-release Tablets, 8 mg, because levels of a diester impurity exceeded the specification limit.
Sophysa is recalling 105 Pressio 2 ICP Monitoring Systems following customer complaints of the Pressio monitor rebooting.
Ziyad Brothers Importing is recalling 2,865 cases of Baraka French Style Puff Pastry because the product may contain partially hydrogenated oils.
AvKARE is recalling 7,991 cartons of Rosuvastatin Tablets, USP 10 mg, because the product was out of specification for dissolution.
Beckman Coulter is recalling 6,457 UniCel DxI 800 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.
Integra LifeSciences is recalling 1,301 Codman Microsensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
SpecGx is recalling 287,988 bottles of Oxycodone and Acetaminophen CII Tablets, 10 mg/325 mg, because of the potential for the imprint to be missing on tablets.
SpecGx is recalling 74,544 bottles of Oxycodone and Acetaminophen CII Tablets, 7.5 mg/325 mg, because of the potential for the imprint to be missing on tablets.
Beckman Coulter is recalling 1,272 UniCel DxI 600 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.
Integra LifeSciences is recalling 5,116 Codman CereLink ICP Sensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.
East Trailers is recalling 2024-2026 Beast and Beast II trailers because an improper weld may cause the rear impact guard to detach, increasing crash injury risk.
Lippert is recalling 3000 Series Hidden Hinge Ramp Doors because they may break away from the frame during use, increasing the risk of injury.
Terex is recalling 2025 TL, LT, LTM40, HR40, HR46, and SCM55 aerial devices because a control valve defect may cause hydraulic equipment to overheat, posing a burn risk.
Jaguar Land Rover is recalling 2026 Range Rover Sport vehicles because the certification label lists incorrect weight information, which could lead to overloading.
Goodyear is recalling specific Cooper Discoverer SRX tires because incorrect Tire Identification Numbers prevent proper registration and compliance with federal safety standards.
About 60,250 DR Power walk-behind and tow-behind leaf vacuums are being recalled because pieces can come loose inside the unit or debris can pierce the chute, ejecting material.
About 4,155 Vasicar 18-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 5,000 Agrish adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
About 320 RH 48-inch and 60-inch Natural Antler Chandeliers are being recalled because canopy hardware can break when hung at an angle, causing the fixture to fall.
About 18,700 Julie and Judah pajama and lounge pants and shorts are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 870 Rattan 6-Drawer Dressers, model YD001, are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 1,430 NFSVLB baby bath seats are being recalled because they are unstable, can tip over, and have leg openings that allow a child's torso to become entrapped.