State
73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
PACCAR is recalling 2015-2021 Peterbilt 320 and 520 trucks because the steering column support may crack, increasing crash risk.
Braun Ambulances is recalling specific Crestline CCL150 ambulances because defective seat belt fasteners may fail, increasing injury risk in a crash.
Marion Body Works is recalling one 2018 Freightliner M2-106 vehicle because a license plate light may be aimed at other drivers, increasing crash risk.
Volvo is recalling 2021 V60, V90, XC60, and XC90 models because the SRS control unit may detach during a crash, reducing occupant protection.
Noble House Home Furnishings is recalling four models of chests, cabinets, and dressers because they are unstable and can tip over, posing serious hazards to children.
John Deere is recalling Frontier rotary tillers because some lack a safety sign warning of entanglement hazards. No injuries have been reported.
Automann is recalling Warning Triangle Sets because their color, reflectivity, and stability may reduce effectiveness, potentially increasing crash risk.
WishGarden Herbs is recalling 298 jars of Goldenseal Powder because testing found Cronobacter Sakazakii contamination.
Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.
Imprimis NJOF, LLC is recalling 6,520 vials of Dexamethasone-Moxifloxacin PF Injection because 13 vials were found with faulty crimps, raising concerns about sterility.
The FDA is recalling specific lots of Covidien TA Auto Suture Vascular Staplers because a damaged internal component may prevent adequate hemostasis or cause tissue damage.
Becton Dickinson & Co. is recalling BD Phoenix PMIC-110 IVDs due to false resistant SXT results with S. aureus, which could impact antibiotic treatment.
Massimo Motor Sports is recalling percussion massage guns sold at Costco because the lithium-ion battery can overheat and cause fires.
Becton Dickinson is recalling BD Phoenix PMIC-107 IVDs because false resistant results for S. aureus could lead to reduced treatment effectiveness.
Fresenius Kabi is recalling 490,633 vials of Ketorolac Tromethamine Injection because particulate matter was found in reserve samples.
FDA is recalling specific lots of Covidien TA Auto Suture Vascular Loading Units due to a damaged internal component that may prevent adequate hemostasis.
Cipla is recalling 284,610 packets of Esomeprazole Magnesium delayed-release oral suspension because the excipient Crospovidone is contaminated with theophylline.
Cipla is recalling Esomeprazole Magnesium for Delayed-Release Oral Suspension 20mg due to cross-contamination with theophylline in the excipient Crospovidone.
A non-sterile Cord Care Powder product was recalled because testing found Cronobacter Sakazakii contamination, posing a potential health risk without confirmed illness reports.
Westmed is recalling 3,000 units of the REF 3102-E Elongated Oxygen Mask because the tube connection may become loose, potentially delaying oxygen therapy.
Becton Dickinson is recalling BD Phoenix PMIC-109 in vitro diagnostic devices because they may produce false resistant results for S. aureus, potentially affecting antibiotic treatment choices.
Cipla is recalling specific lots of Esomeprazole Magnesium delayed-release oral suspension because the excipient Crospovidone is contaminated with theophylline.
Roche is recalling cobas 8000 modular analyzers because configuration settings may change, causing incorrect results that could go undetected.
Boston Scientific is recalling 458 Contour VL Variable Length Ureteral Stents because trace amounts of nickel particles were found on the devices.
Medtronic is recalling Ares Antibiotic-Impregnated Catheters due to a potential seal defect that may compromise sterility and increase the risk of post-operative infection.