State
73,096 recalls have nationwide distribution and so reach Wyoming. 3,226 additional recalls listed Wyoming specifically in their distribution scope.
Of the 3,226 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 549 (17%) are Severe.
Which agencies issued them
These figures cover only the 3,226 recalls whose distribution notice names Wyoming specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Eugia US LLC is recalling medroxyprogesterone acetate injectable suspension (150mg/mL) due to manufacturing practice deviations. This voluntary recall affects 19,872 vials distributed nationwide.
Greiner Bio-One GmbH is recalling VACUETTE SAFELINK blood collection holders because the protective rubber sleeve may bunch up and fail to retract, causing potential blood leakage from the device.
Certain Tec 6 Plus and Tec 800 series anesthesia vaporizers may deliver less anesthetic agent than the dial setting indicates due to a manufacturing issue. Approximately 1,573 units are affected, distributed in the United States and globally.
Eugia US LLC is recalling Progesterone Injection due to a market complaint of glass particles found in vials. The affected batch poses a potential risk to patients who receive injections from contaminated vials.
Amerisource Health Services LLC is recalling Clobazam 10 mg tablets due to the presence of foreign tablets or capsules in some packages. The recall affects 5,178 cartons with Lot #1019594 distributed nationwide.
Granules Pharmaceuticals is recalling Colchicine 0.6 mg capsules nationwide due to failed dissolution specifications detected during stability testing. Patients should contact their healthcare provider for guidance.
Aerin Medical is recalling 479 units of VivAer Stylus (Lot #10235) due to incorrect programming in units from a single lot. When connected to the Aerin Console, affected devices will be incorrectly identified as RhinAer Stylus.
Jubilant Draximage is recalling 5,209 kits of Technetium Tc 99m Sulfur Colloid Injection that failed stability specifications. The affected lots (C2300070, C2300070E) were distributed nationwide.
Rising Pharma is recalling certain batches of Duloxetine Delayed-Release Capsules 30 mg due to a manufacturing deviation that resulted in elevated N-nitroso-duloxetine impurity above FDA's recommended interim limit.
IDS LTD is recalling 23 Smaxel Fractional CO2 Laser systems worldwide due to missing Certification label and inadequate instructions for safe operation.
Fresenius Medical Care is recalling Dialyzer Optiflux 160NRe units nationwide due to potential internal blood leaks caused by cracked polyurethane in the dialyzer material.
West-Ward Columbus is recalling Methadone Hydrochloride Tablets, 5mg, in unit-dose packaging due to illegible product identification on individual tablets. Lot AC2556A was distributed nationwide.
GKN Automotive is recalling replacement driveshafts for specific BMW Mini and Land Rover models because they can crack or break, increasing the risk of a crash.
Palfinger is recalling 2017-2025 GLS 55 and FHS 55 forklifts because rear marker lights are installed in the wrong location, reducing visibility.
Forest River is recalling 2025 Shasta Oasis and Spirit travel trailers because a cracked burner tube may cause a gas leak and fire risk.
Winnebago is recalling certain 2025 Minnie Winnie and Spirit motorhomes because the spare tire carrier mounting bolts may loosen, allowing the carrier to detach.
Kia is recalling certain 2024-2025 Sorento vehicles because a Body Domain Control Unit software error may cause a loss of low beam headlights and taillights.
N&B Mobility Solutions is recalling Nivion NSP01 charger adapters due to electrical arcing and shock risks. Owners should contact Nivion for a free replacement.
Bestway Sandwiches Inc. is recalling frozen chicken and cheese taquitos due to possible metal contamination. One consumer reported a dental injury.
Kowalski's Garden Salad (14 oz) is recalled due to potential Salmonella contamination in cucumbers. The recall affects 206 units distributed across 11 states with use/sell by dates November 6-15, 2024.
Sprouts Farmers Market is recalling Sprout Gyro Family Kit due to potential Salmonella contamination in the tzatziki sauce. The product was distributed across 23 states.
Reser's Fine Foods is recalling FCF Item 404885 Gyro Kit No Trays due to potential Salmonella contamination from implicated cucumber in the tzatziki sauce cups. The product was distributed to consignees in 19 states.
GNMart LLC is recalling FORCE FOREVER 400mg tablets nationwide after the FDA found the product contains undisclosed Diclofenac and Dexamethasone. The Class I recall affects all lots of this dietary supplement product.
RUSS DAVIS WHOLESALE is recalling Bacon Avocado Wraps sold under Crazy Fresh and quick & easy brands due to potential Salmonella contamination in cucumbers. 491 units were distributed across 11 states.
Heber Valley Artisan Cheese is recalling Cascade Raw Cheddar Cheese due to Shiga toxin-producing E. coli (STEC) and elevated E. coli detected in finished products. The affected cheese was sold in MT, NV, UT, and WY.