State
73,100 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, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 939 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Terex is recalling 2020-2024 XT Pro vehicles because replacement basket brackets may cause the basket to tilt, risking occupant falls.
Claire's and Icing stores are recalling about 5,700 Halloween witch hats sold nationwide from July through December 2023. The hats violate federal flammability requirements and pose a risk of burn injuries.
JUVENNO KIDS is recalling about 18,620 children's button-up pajama sets sold on Temu.com because they violate federal flammability standards for sleepwear and pose a burn injury risk to children. No injuries have been reported.
Lovely Angel children's lace nightgowns sold on Temu.com violate federal flammability standards for sleepwear, posing a burn injury risk to children. About 4,360 units were sold between June 2023 and May 2024.
About 45,300 children's two-piece pajama sets sold on Temu.com violate federal flammability standards for sleepwear, posing a burn risk to children. Consumers should immediately stop using the garments and contact Fashion Online for a refund.
TonGass 8-inch round pool drain covers do not meet Virginia Graeme Baker Pool and Spa Safety Act standards and pose an entrapment hazard to swimmers and bathers. About 1,650 units sold on Amazon from September 2023 through June 2024 are affected.
Ross Stores is recalling about 1,600 metal-framed armchairs because the chair legs can bend or break, posing fall and injury hazards. The company has received five reports of broken legs, four of which resulted in minor injuries.
Megadyne Medical recalls MEGA SOFT reusable patient return electrodes (Model 0830) due to identified burn risk. Use is restricted to patients aged 12 and older.
Integrity Products recalls RAM IT Horny Goat Weed dietary supplement capsules nationwide because they contain undeclared sildenafil, a prescription drug not listed on the label.
MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrodes are recalled due to an identified risk of patient burns. Use should be restricted to patients aged 12 or older.
Walmart Great Value Organic Black Chia Seeds (32 oz) are being recalled due to potential Salmonella contamination. The product was distributed to multiple states.
Megadyne is recalling the MEGA 2000 Patient Return Electrode due to identified potential risk of patient burns. Use is now restricted to patients aged 12 or older.
To the Moon Capsules are being recalled nationwide because they contain undeclared sildenafil, a prescription pharmaceutical. The product was marketed without FDA approval.
SeaSpine Orthopedics is recalling Fathom Pedicle-Based Retractor C/C Blades due to manufacturing defects that could cause bone fracture. The recall affects 31 units distributed across nine US states.
Medline Industries recalls 7,673 surgical convenience kits due to weak Pure Pouch seals that may compromise sterility. Kits were distributed nationwide to healthcare facilities.
Trigen Laboratories recalls Methylphenidate Hydrochloride Extended-Release Tablets (36mg) because a batch failed dissolution specifications. Approximately 10,448 bottles were distributed nationwide.
Medline surgical convenience kits containing Pure Pouch components with weak seals may fail to maintain sterility, potentially compromising the safety of contained medical instruments. Affected kits were distributed nationwide across 23 states.
Medisca Inc. is recalling 113 bottles of Budesonide, USP (Micronized) 500 mg due to glass particulate matter contamination caused by manufacturing deviations. The product was distributed nationwide in the USA and Canada.
First Source Inc is recalling the First Source Vision M portable X-ray cart because the bolt securing the positioning arm to the gas spring may come loose and fall onto a patient.
Angiodynamics is recalling IsoLoc Prostate Immobilization Balloons (ISO-100, Lot 5402) for mislabeling. Devices have 100cc fill volume but are labeled as ISO-60 (60cc).
Little Moon Essentials voluntarily recalls Dream Cream due to manufacturing quality control violations. No illnesses reported.
Italiamo brand frozen Eggplant Parmesan may contain undeclared wheat and milk allergens. Foreign language labeling prevented proper allergen disclosure.
BD Pyxis automated dispensing cabinets were shipped with socket-outlet power strips that lack IEC electrical certification, potentially exposing users to leakage currents and electric shock.
Abbott Liberta RC implantable pulse generators used for deep brain stimulation may unexpectedly turn off approximately every 50 days after activation, resulting in loss of therapy. Approximately 302 units have been recalled nationwide.
BD Pyxis MEDBANK medication cabinets contain power strips not certified to electrical safety standards, potentially exposing users to leakage currents. The recall affects 677 units distributed nationwide.