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.
Mercedes-Benz is recalling 2019 GLA 250 vehicles because the transmission control unit power supply may interrupt, causing the vehicle to shift into neutral while driving.
Mercedes-Benz is recalling 2017-2021 C300, AMG C43, and AMG C63 vehicles because front seat belts may not fully retract, potentially discouraging use and increasing crash injury risk.
Smeal is recalling 2009-2020 Aerial Fire Apparatus vehicles because a defective trolley can detach from the ladder, posing a risk of injury or death.
Chrysler is recalling certain 2021 Jeep Gladiator vehicles with manual transmissions. The clutch pressure plate may overheat and fracture, increasing the risk of fire and potential loss of drive.
Autocar is recalling certain 2018-2021 Xpeditor vehicles because the seat belt harness may chafe and short circuit the engine, causing unexpected stalling that could lead to crashes.
Penumbra Inc. is recalling 3,368 JET 7 Reperfusion Catheters because the distal tip may become damaged during use, posing a risk of vessel damage and patient injury or death.
Penumbra Inc. is recalling JET 7 Reperfusion Catheters because distal tip damage could cause vessel injury or death during use.
Penumbra Inc. is recalling JET 7 Reperfusion Catheters because distal tip damage could cause vessel injury or death during use.
Penumbra Inc. is recalling JET 7MAX Kits because catheter tip damage during use could cause vessel damage, leading to patient injury or death.
Edge Pharma, LLC is recalling 48 syringes of Ceftazidime Sterile Ophthalmic Solution because the media used for sterility testing was expired, compromising the assurance of sterility.
Steris is recalling Reliance Vision Single-Chamber Washer/Disinfector units because a faulty electrical contactor may cause the drying chamber to overheat, potentially leading to smoke or fire.
Laerdal Medical is recalling 5,035 Compact Suction Units (LCSU 4) because component failures may cause the device to lose suction, potentially delaying treatment or causing suffocation.
Audi is recalling one 2019 Q3 vehicle because a production deviation may prevent a steering component from engaging properly, increasing the risk of a crash.
Front steering knuckles in certain Volkswagen Atlas and Atlas Cross Sport vehicles may fracture, causing loss of vehicle control and increasing crash risk. Volkswagen will inspect and replace affected knuckles free of charge.
Medtronic is recalling 95 Neonatal Delta Valve Shunt Assemblies because a manufacturing defect may cause the ventricular catheter to disconnect from the valve, leading to shunt malfunction.
Medtronic is recalling specific Neonatal Delta Valve Shunt Assemblies because a manufacturing defect may cause the ventricular catheter to disconnect, leading to shunt malfunction.
Medtronic is recalling Neonatal Delta Valve Shunt Assemblies because a manufacturing defect may cause the ventricular catheter to disconnect from the valve, leading to shunt malfunction.
Complete Pharmacy and Medical Solutions is recalling 1,144 vials of Human Chorionic Gonadotropin 5,000 IU because the product lacked required potency testing.
American Health Packaging is recalling 1,948 cartons of Nitrofurantoin Capsules USP 100 mg because they failed dissolution specifications. The recall is nationwide.
CB2 is recalling Junction Tall Chests and Low Dressers because they can tip over or entrap children if not anchored to the wall.
Complete Pharmacy and Medical Solutions is recalling 1,182 vials of Human Chorionic Gonadotropin because the product lacked required potency testing.
Biomet is recalling 174 A.L.P.S. Clavicle Plating Systems because instruments may cold weld, preventing disassociation and increasing the chance of drill fracture.
Fujifilm is recalling Synapse PACS Software versions 5.1 and higher because it may display incorrect patient information or PET/CT values.
Abbott Point Of Care Inc. is recalling i-STAT EG7+ cartridges because the ionized calcium test may report higher than expected results if stored at room temperature for specific periods.
Boston Scientific is retrieving five ACUITY Universal Cutters that did not undergo the required sterile processing procedure.