State
73,596 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,438 recalls naming Delaware we have scored against our rubric, 475 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,112 (32%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it failed potency testing. Patients should consult their healthcare provider.
Hostess Brands is recalling 34,409 cases of Raspberry Zingers cakes nationwide due to potential mold growth prior to the best-by date.
Flower Orthopedics is recalling 25 calcaneus plates because the manufacturer used a titanium alloy instead of pure titanium.
HF Acquisition Co. LLC is recalling two STAT KIT Z-1000 emergency medical kits because they are missing a hand suction pump component.
Teva Pharmaceuticals is recalling Lidocaine 5% Patches because individual pouches are missing lot and expiration dates. The recall covers 28,596 cartons distributed nationwide.
Flower Orthopedics is recalling 25 Calcaneus Plates, Extensile, Large, Right (Catalog Number CPF 203) because the contract manufacturer used a titanium alloy instead of pure titanium.
Taro Pharmaceuticals is recalling specific lots of Clobetasol Propionate Cream 0.05% because the bulk material failed content uniformity testing.
Lupin Pharmaceuticals is recalling Mibelas 24 Fe chewable tablets because they failed impurity specifications. The recall covers 560,922 pouches distributed nationwide.
Intrinsic Therapeutics is recalling 110 units of Barricaid Annual Closure Devices because the inner container labels display the wrong catalog number.
Wright Medical Technology is recalling 66 hardware removal kits because they lack the specific drivers needed to remove Dart-Fire 2.5 and 3.0mm Headless screws.
Smith & Nephew is recalling 3 units of a PeriLoc Targeter handle that was incorrectly marked as a left-hand part.
Flower Orthopedics is recalling 25 calcaneus plates because they were manufactured with a titanium alloy instead of pure titanium.
Eosera, Inc. is voluntarily recalling 125,874 bottles of Ear Pain MD Pain Relief Drops with 4% Lidocaine due to current Good Manufacturing Practice (cGMP) deviations.
Wright Medical Technology is recalling 9 units of the Screw Removal Case Assembly because the kits do not include drivers required to remove specific headless screws.
NeuroLogica is recalling 35 OmniTom CT systems due to potential operational issues that could cause inadvertent shutdowns and delays in patient treatment.
Linet Americas is recalling 202 AVE 2 Birthing Beds because the Unique Device Identifier (UDI) on the label indicates the incorrect manufacturer.
Golden State Medical Supply Inc. is recalling specific lots of Clobetasol Propionate Cream, USP, 0.05% because the bulk material failed content uniformity testing.
Faribault Foods is recalling 14-oz. cans of Progresso Organic Chicken Noodle Soup because the product contains undeclared milk, soy, beef, and pork.
BMW is recalling hybrid X3, 330e, X5, and 2020 MINI Countryman SE models with loose battery welds that may cause short-circuits and fire. All vehicles have already been remedied.
Heartland Recreational Vehicles is recalling 2021 Mallard travel trailers because the liquid propane hose and connector may contact the suspension shackle, increasing the risk of fire.
KME is recalling 38 fire trucks because certain LED lights are too bright, potentially blinding other drivers and increasing crash risk.
Forest River is recalling specific 2017-2020 motorhomes because a damaged Power Distribution Module may cause rear marker, brake, or turn signal lights to stop working.
Watson & Chalin is recalling SL2065 steerable lift axle suspension systems because short pivot cap screws may separate, creating road hazards and increasing crash risk.
General Motors is recalling 2020 Chevrolet Corvette vehicles because the front trunk lid can be driven while unlatched, potentially opening at speed and obstructing the driver's view.
Forest River is recalling 2016-2020 Coachmen motorhomes because the awning may deploy while the vehicle is moving, increasing crash risk.