State
73,570 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 1,110 (32%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
SmartPool is recalling Bee Free children's helmets because they do not meet safety standards for children under 5, posing a risk of head injury.
Confirm Biosciences is recalling Orient Gene COVID-19 Rapid Test Cassettes because they were distributed outside Emergency Use Authorization and not validated for fingerstick use.
Volvo is recalling 2021-2022 XC40 Recharge vehicles because a battery software defect may cause the high-voltage system to disconnect, increasing crash risk.
Urban Outfitters is recalling Margo Taper Candle Holders because they can catch fire if they contact the flame. One fire incident was reported, with no injuries.
Getinge is recalling CM320 Series Washer Disinfectors because plastic inlet hose connections may deform or break, potentially causing water leaks and burns.
Biomet is recalling 49 units of 25mm central screws for shoulder prostheses because they were mislabeled as 25mm but are actually 40mm.
Polestar is recalling certain 2021-2022 Polestar 2 vehicles. A software issue in the Battery Energy Control Module may cause the high voltage system to disconnect, resulting in loss of drive power and increased crash risk.
Carl Zeiss Meditec is recalling 613 IOLMaster 700 devices because software versions 1.90.2.09 and 1.90.8.06 may display incorrect patient information when using the modality worklist.
Northern Tool & Equipment is recalling Powerhorse 13000ES portable generators due to a wiring error that can cause electrical shock. No injuries have been reported.
GE Healthcare is recalling 96 Revolution CT systems because a damaged or missing table pinch protector may expose sharp screws, posing a laceration risk.
GE Healthcare is recalling Revolution CT and Revolution CT ES systems because damaged or missing table pinch protectors may expose sharp screws, posing a laceration risk.
Potter Electric is recalling specific addressable pull stations because the handle may fail to activate the fire alarm, posing a risk of failure to alert occupants to a fire.
Daimler Trucks North America is recalling 2021-2022 Freightliner Custom XC Chassis vehicles because a missing brake pedal return spring may cause brake lights to stay on or brakes to remain engaged.
Daimler Trucks North America is recalling 2022 Thomas Built Minotour School Buses because the engine can start while an emergency exit is locked, delaying evacuation.
Audi is recalling certain 2019-2021 A8 and 2020-2021 S8 vehicles due to a missing sealing pin on the engine control module connector. Moisture can enter the connector and cause the engine to stall, increasing crash risk.
Medtronic Neurosurgery is recalling 22,528 units of STRATA II cerebrospinal fluid valves and shunts worldwide because radiopaque markings may vary in visibility under imaging.
Confirm Biosciences is recalling Healgen COVID-19 Rapid Test Cassettes because they were distributed to non-certified labs and not validated for fingerstick use.
Cairn Diagnostics is recalling 103 kits of the 13C-Spirulina Gastric Emptying Breath Test due to a potential for false negative diagnoses of gastroparesis.
DLC Laboratories is recalling 86,297 jars of Sulfur Ointment 10% because English labels for Camphor were incorrectly applied to the product.
Ascend Laboratories LLC is recalling Cephalexin for Oral Suspension due to CGMP deviations involving unidentified impurities.
Akebia Therapeutics is recalling Auryxia (ferric citrate) tablets because they failed to meet dissolution specifications.
Ascend Laboratories is recalling Cephalexin for Oral Suspension because unidentified impurities were found at higher levels than allowed.
Medtronic is recalling Delta CSF flow control valves because radiopaque markings may not be clearly visible under X-ray imaging.
Medtronic Neurosurgery is recalling 20,817 CSF-Flow Control Valves worldwide due to potential variation in radiopaque marking visibility under radiographic imaging.
Sky Medical Supplies and Equipments LLC is recalling 10,000 SARS-CoV-2 rapid test kits distributed in Florida and Peru because they were sold without FDA Emergency Use Authorization.