State
73,503 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.
Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,083 (39%) are Severe.
Which agencies issued them
These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
H&M is recalling about 615 children's sleepwear sets sold online from October to November 2021 because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Lovevery is recalling steel drinking cups with handles included in Inspector Play Kits because the handle can detach, posing a choking hazard to young children. About 169,000 units were sold online from July 2018 through July 2021.
Zeno collapsible infant walkers fail to meet federal safety standards and pose fall and neck entrapment risks to babies. Consumers should stop using the walkers immediately and contact Zeno for a free return and refund.
Navistar is recalling 2019 International LT and RH vehicles because the LED backup lights are the wrong color, failing federal safety standards.
Morgan Foods is recalling Skyline chili cans that contain undeclared milk, wheat, and soy allergens. The product may actually be cream of chicken soup.
Siren Snacks recalls Siren Birthday Cake Protein Bites for undeclared cashews and almond butter allergens that may pose a risk to consumers with nut allergies.
E25Bio COVID-19 diagnostic tests have been recalled following nationwide distribution without FDA authorization or approval. The distributed units lacked sufficient directions and quality controls needed for safe diagnostic use.
Ford is recalling certain 2021-2022 E-350 and E-450 vehicles with dual rear wheels due to inadequate power steering line connections. This defect may cause sudden loss of power steering fluid, resulting in loss of steering and brake assist.
Conagra Brands is recalling Wishbone Chunky Blue Cheese Dressing due to undeclared eggs on the label. Consumers with egg allergies should not use this product and should return or dispose of any affected bottles.
Junp Hydration LLC is recalling MegMan Performance Booster 800 mg capsules because the product contains undeclared tadalafil, an active pharmaceutical ingredient not listed on the label, making it an unapproved drug.
Conagra Brands is recalling Wishbone Thousand Island Dressing due to undeclared eggs. The recall affects 4,971 cases distributed to retailer distribution centers nationwide.
AuroMedics Pharma LLC is recalling Polymyxin B for Injection USP (Lot CPB200013) nationwide due to the presence of particulate matter, including hair, found in vials.
HARD DAWN Rise and Shine capsules (500 mg) are being recalled because they contain tadalafil, an FDA-approved drug, without proper approval or labeling. The product was sold nationwide via Amazon.
GE Healthcare is recalling 17,228 MR superconducting magnet systems because the cryogenic ventilation system may not meet required venting standards.
Microbiologics Inc is recalling KWIK-STIK QC Sets and Panels due to potential contamination with E. coli and Staphylococcus species. The affected product was distributed worldwide to laboratory testing facilities.
The Novalung Sensor Box may experience communication failures between its flow sensor and sensor box component, potentially disabling flow measurement and air bubble detection. The recall affects 115 units distributed across 16 US states.
Smith & Nephew is recalling the Acufex Access Advanced Positioning Kit because the products were shipped to a distribution center instead of the sterilizer and were not sterilized before distribution.
GE Healthcare Discovery MR450 MRI systems may have cryogen ventilation systems that do not meet required venting standards. The recall affects approximately 17,228 devices distributed in the U.S. and internationally.
GE Healthcare recalled 17,228 superconducting magnets, a component of SIGNA 1.5T MR systems, due to a cryogen ventilation system that may not meet venting requirements. Systems are distributed nationwide and internationally.
GE Healthcare is recalling approximately 17,228 SIGNA Creator and Explorer MRI systems due to potential defects in their cryogen ventilation systems that may not meet required venting standards.
GE Healthcare is recalling MRI superconducting magnets with cryogen ventilation system defects not meeting safety requirements. The recall affects 17,228 devices distributed across the US and internationally.
GE Healthcare is recalling 17,228 MR superconducting magnet components due to a cryogen ventilation system that may not meet required venting specifications.
Diagnostic control microorganisms manufactured by Microbiologics Inc are recalled for returning incorrect antibiotic susceptibility test results. These controls failed quality specifications and could cause inaccurate lab test results.
Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy (PEG) Kit because the external retention bolster may be oversized relative to the tube. Approximately 2,652 units have been distributed in the US, Canada, and Chile.
GE Healthcare is recalling Discovery MR750w 3.0T MRI systems due to cryogen ventilation systems that may not meet FDA venting requirements. Approximately 17,228 devices were affected.