State
73,576 recalls have nationwide distribution and so reach Connecticut. 6,572 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,572 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,881 (29%) are Severe.
Which agencies issued them
These figures cover only the 6,572 recalls whose distribution notice names Connecticut specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Elektron Power Handle BP-1 units can short circuit and overheat, creating fire and burn risks. Consumers should stop using them immediately and contact Elektron for a full refund.
Lupin Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to failed water loss tests that may affect drug concentration. The recall affects 16,272 bottles distributed nationwide.
Ultra Seal Corporation is recalling Afassco Pain Free Plus X-Strength Pain Reliever tablets nationwide due to out-of-specification results for Salicylic Acid, a related compound of Aspirin, indicating failed stability testing.
MacLeods Pharma USA is recalling Rizatriptan Benzoate Film Coated Tablets (10 mg) due to out-of-specification test results in organic impurities testing. The recall affects multiple lot numbers distributed nationwide.
Ultra Seal Corporation is recalling Xpect First Aid Extra Strength Pain Away tablets nationwide due to out-of-specification results for Salicylic Acid, a compound related to Aspirin, indicating failed stability testing.
Ultra Seal Corporation is recalling Advance Formula Pain Reliever tablets (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) distributed nationwide due to out-of-specification results for Salicylic Acid, an Aspirin-related compound.
Ultra Seal Corporation is recalling North by Honeywell Pain Stopper Extra Strength tablets nationwide because stability testing found out-of-specification results for Salicylic Acid, an aspirin-related compound.
W L Gore & Associates is recalling GORE CARDIOFORM Septal Occluder devices labeled with a 3-year expiration date instead of the correct 2-year date. Mislabeling could result in use of devices beyond their intended safe lifespan.
Ultra Seal Corporation is recalling AERO Tab Pain Reliever tablets nationwide because out-of-specification results were found for Salicylic Acid, an Aspirin-related compound, indicating failed stability testing.
Sun Pharmaceutical Industries is recalling 22,752 blister packs of Loratadine-D Extended-Release Tablets (10mg/240mg) distributed nationwide due to failed moisture limits. The affected lot is AC14635 with expiration date 12/2022.
Ultra Seal Corporation is recalling PainAway II tablets nationwide due to failed stability specifications. Testing found out-of-specification levels of Salicylic Acid, an aspirin-related compound.
W. L. Gore & Associates is recalling GORE CARDIOFORM Septal Occluders labeled with incorrect 3-year expiration dates instead of 2-year dates. This labeling error affects devices distributed across the United States and internationally.
GORE CARDIOFORM SEPTAL OCCLUDER devices are recalled for labeling errors: 95 units marked with 3-year expiration instead of correct 2-year date. Affected units distributed across US and international locations.
Ultra Seal Corporation is recalling ZEE+ Painaid ESF Extra-Strength Formula tablets nationwide due to out-of-specification results for Salicylic Acid, an aspirin-related compound. The recall affects 50-count and 125-count packages with lot numbers AK-9547 (exp. April 22) and AK-9941 (exp. December 22).
Macleods Pharma USA is recalling Rizatriptan Benzoate 10mg orally disintegrating tablets nationwide due to out-of-specification results in organic impurities testing of controlled samples.
SUN PHARMACEUTICAL INDUSTRIES INC is recalling Kirkland Signature AllerClear D 24 HR (Loratadine and Pseudoephedrine Sulfate) tablets nationwide because the product failed to meet moisture content limits.
Ultra Seal Corporation is recalling Vica-Cet Back Pain Relief tablets nationwide because certain lots failed stability testing and contain out-of-specification levels of Salicylic Acid, an aspirin-related compound.
Daimler Trucks is recalling 1,434 Thomas Built school buses because a loose alternator cable connection may cause electrical arcing and increase the risk of a fire.
FCA US is recalling 2020 Alfa Romeo Giulia vehicles because some may have tires with a lower load rating than intended, increasing crash risk.
Oshkosh is recalling 2020-2021 S-Series vehicles because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of steering assist.
Heartland Recreational Vehicles is recalling 2019-2021 Road Warrior and 2020-2021 Cyclone trailers because wire securement lugs may be improperly tightened. Loose wires can cause electrical arcing and increase fire risk.
Kia is recalling 2017-2018 Optima Hybrid and Plug-In Hybrid vehicles because premature engine bearing wear can cause engine damage, increasing the risk of fire or a crash.
Axalta Coating Systems is recalling windshields that may not be adequately bonded to Ford and Chrysler vehicles due to a coating defect.
Mercedes-Benz is recalling 2021 S 580 and Maybach S 580 vehicles because a software error may cause the engine to stall without restarting, increasing crash risk.
Thor Motor Coach is recalling 2017 Outlaw, Challenger, and Miramar motorhomes because external compartment door skins may separate during transit, creating a road hazard.