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.
Home Easy is recalling about 3,000 Geek Heat DH-QN06 personal heaters because the toggle power switch can spark and cause a fire. The company has received three reports of fires caused by the switch, though no injuries or property damage have been reported.
DIXI Medical Microdeep Depth Electrodes are recalled due to potential deformation of the blister pack packaging that could compromise the sterile barrier. 345 units nationwide are affected.
DIXI Medical is recalling 484 Microdeep Depth Electrodes nationwide due to potential deformation of internal packaging that could compromise the sterile barrier of these brain recording devices.
Immuno-Mycologics recalls 411 Cryptococcal Antigen test kits (lots F1021035, F1021036) for reduced specificity (90% vs. 99%), which may cause false-positive results leading to unnecessary anti-fungal therapy.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because the gross vehicle weight rating may be incorrectly stated on the tire and loading label.
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes used in neurological monitoring and stimulation due to potential deformation of the internal sterile packaging. The compromised sterile barrier could allow contamination before use.
Luminex Corporation is recalling ARIES HSV 1&2 Assay cassettes (lot numbers AB3600A and AB3560A) due to a confirmed 0.9% leak rate. Leaking cassettes may cause incorrect or delayed test results.
Philips is recalling certain versions of eCareManager software because the Sentry Score feature was not approved by FDA prior to distribution. Users should contact Philips for updated information.
Stack Em' Up Books is recalling Adam the Apple children's stackable toys because the surface paint contains lead levels that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health effects.
FEMSelect Ltd is recalling 141 units of the EnPlace trans-vaginal pelvic floor repair system because certain lots may not have been packaged with the required Channel Tube Limiter accessory.
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential packaging deformation that could compromise the sterile barrier. Approximately 2,720 units were distributed nationwide for use in brain recording and stimulation procedures.
BMW is recalling certain 2022 330i, 530i, X3, and X4 vehicles because the transmission mechatronics unit may not have been properly assembled, potentially causing an internal leak that could lead to vehicle rollaway and crash risk.
DIXI MEDICAL USA is recalling 461 Microdeep Depth Electrodes. The internal blister packaging may deform, potentially compromising the sterile barrier when removed from the protective Tyvek bag.
Hyundai recalls 2021 Accent vehicles due to defective seat belt pretensioners that may explode in a crash and project metal fragments, risking injury to occupants.
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential deformation of the internal packaging (blister pack) that could compromise the sterile barrier. The recall affects 365 units distributed nationwide.
DIXI Medical USA is recalling 2,141 Microdeep Depth Electrodes nationwide due to potential deformation of the blister pack that could compromise the sterile barrier when devices are removed from their Tyvek bags.
Maintainer is recalling 2021-2022 truck-mounted cranes because an incorrectly installed guard may damage fuel hoses or cables, increasing fire risk.
Petzl is recalling about 230 Scorpio Eashook Lanyards with Carabiners because the carabiner's automatic gate-closing system can malfunction, creating a risk of serious injury or death.
Smith & Nephew recalls INTEGRA SURFIX ALPHA Screwdriver Torx 10 units because they are out of specification and may not mate properly with the Surfix Alpha Lock screw.
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes nationwide due to potential internal packaging deformation that could compromise the device's sterile barrier.
Escalade Sports is recalling about 5,200 tennis tables sold at Target from September to November 2021 because the table can collapse when leaned against, posing a fall hazard. The company has received 78 reports of collapse, including four reports of minor injuries.
Software error in certain Siemens ACUSON Sequoia ultrasound systems causes measurement values to be overestimated, potentially resulting in patient misdiagnosis.
Altec is recalling 2019-2021 ATTXX-M/P/S aerial devices because over-tightened bolts in the rotation bearing may break, risking separation of the pedestal and turntable.
DIXI MEDICAL USA is recalling 1792 Microdeep Depth Electrodes due to potential deformation of the internal blister pack that could compromise the sterile barrier when the device is removed from its Tyvek bag.
The Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm has a protector sleeve that may be difficult to remove, potentially damaging the balloon and causing patient harm. Covidien is recalling 1,994 devices.