State
72,940 recalls have nationwide distribution and so reach Delaware. 3,435 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,435 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 937 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,435 recalls whose distribution notice names Delaware specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 15,000 Modera Pack N Play play yard mattresses are being recalled because they may not fit certain play yards, creating gaps that pose a deadly entrapment hazard.
Autocar is recalling 2025-2026 Xpeditor vehicles because the Automatic Emergency Braking system may unexpectedly turn off when the vehicle turns, increasing crash risk.
Remote Vans is recalling 2025 Aegis and Oasis motorhomes because optional equipment may cause the vehicles to exceed their Gross Vehicle Weight Rating, increasing crash risk.
About 6,600 Destination Holiday Glow Light Stick bracelet 12-packs are being recalled because the green bracelet can leak, posing a skin irritation hazard.
Sprouts Farmers Market is recalling Smoked Mozzarella Pasta Salad sold at deli counters and in grab-and-go containers because the product may contain Listeria monocytogenes.
Abiomed is recalling Automated Impella Controllers over the potential for purge pressure issues caused by purge retainer failures, covering 9,177 distributed units.
M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.
Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.
M.C.I. Foods is recalling 330 cases of Cheese and Egg with Green Salsa Breakfast Burritos after the cooked egg ingredient tested positive for Listeria monocytogenes.
ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.
B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.
Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.
Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.
Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.