State
73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
American Outdoor Brands is recalling Caldwell E-Max Pro BT Earmuffs with rechargeable lithium battery packs due to a soldering defect that can cause the unit to overheat, posing fire and burn hazards. No injuries have been reported.
C-RAD POSITIONING AB is recalling Catalyst positioning software c4D because it fails to properly update the Site field during synchronization in the setup workflow. This software defect may prevent correct system configuration.
Canon Vantage Tiitan 1.5T MRI Systems with certain serial numbers are recalled due to a component lacking proper flame retardancy, which could result in smoke or fire.
Nissan is recalling 2021 Rogue Sport vehicles because seat belt automatic locking retractors may deactivate prematurely, reducing protection for child safety seats and violating federal crash protection standards.
Cordis Corporation is recalling 680 Avanti® Catheter Sheath Introducer units because the actual product dimensions are larger than the labeling indicates.
Bea Lydeckers Naturals Inc is recalling Living Free "Adult Extra" multi-vitamin capsules because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.
Bea Lydeckers Naturals Inc is recalling Living Free Heart/Blood Vessel Dietary Supplement because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.
Bea Lydeckers Naturals Inc is recalling Living Free Immune Dietary Supplement because the label declares lecithin but does not declare that it contains soy lecithin, posing a risk to consumers with soy allergies.
Arrow International is recalling 4 units of an electrode catheter marketed without FDA 510(k) clearance. The device was intended for electrophysiology studies.
Canon Medical System recalled its Vantage Titan 3T MRI systems due to a component lacking proper flame-retardancy standards. The defect could produce smoke or fire during use.
Kalmar is recalling 2021 Ottawa T2 vehicles because an incorrectly installed rear stability control harness may cause the system to be inactive, increasing crash risk.
Bea Lydeckers Naturals Inc is recalling Living Free Lung & Joint Congestion Herbal Dietary Supplement because the label declares lecithin but does not identify it as soy lecithin, creating an undeclared soy allergen hazard.
Bentley is recalling certain 2020-2021 Continental GT vehicles because the front seat may trap a rear passenger's legs during automated movements. The front seat software will be updated free of charge.
Bea Lydeckers Naturals Inc is recalling Living Free Nerve & Muscle Plus Cetyl-Myristoleate supplement because the label declares lecithin but does not declare that the lecithin is soy-derived, posing a risk to consumers with soy allergies.
Rite Aid is recalling about 9,780 rechargeable handheld fans sold nationwide from April through June 2021 because the lithium ion battery can overheat while charging and pose a fire hazard. The company has received two reports of the fans overheating and emitting smoke, though no injuries have been reported.
Sanit Technologies, LLC is recalling Durisan Antimicrobial Solutions Hand Sanitizing Wipes (benzalkonium chloride, 0.13%) due to manufacturing deviations that could result in contaminated product.
Arrow International is recalling its Temporary Pacing Catheter/Introducer Kit (5 units) because it was marketed without FDA 510K clearance. Affected lot numbers: 16F20C0035 and 16F20F0124.
Sanit Technologies, LLC is recalling multiple lots of Durisan Antimicrobial Solutions hand sanitizer due to manufacturing deviations. The affected products were manufactured under the same conditions as contaminated lots.
Cipla USA is recalling 7,228 bottles of Solifenacin Succinate Tablets, 10 mg (Lot #GG90819, expiring 06/2021) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Mercedes Medical voluntarily recalled Lingen SAMPLE Virus Sampling Kits due to lack of FDA 510(k) clearance. The recall affects units distributed nationwide and internationally.
The Lingen Disposable Virus Sampling Kit by Mercedes Medical was voluntarily recalled due to lacking FDA 510(k) clearance. The recall affected approximately 11,711 boxes distributed nationwide and internationally.
Trail King is recalling 2018-2020 TKOLB trailers because the steering arm may detach, increasing crash risk.
Newell Coach Corp. is recalling 2008-2022 P50 vehicles because window vent adhesive may fail, causing the vent to detach and increasing crash risk.
Certain 2022 Kenworth T680, T880, and W990 trucks have defective HVAC controls that may fail to operate the windshield defrost system, reducing driver visibility and increasing crash risk. PACCAR is replacing the HVAC control heads free of charge.
Newmar Corporation is recalling certain 2021 Ventana motorhomes because tie rod clamps may be loose, potentially causing tie rod ends to break or detach and resulting in steering loss.