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.
JMH International is recalling Chef Myron's Premium Shoyu Sauce because it contains wheat-derived gluten despite a gluten-free claim.
BRP is recalling Can-Am Off-Road screw jacks because they can collapse, posing a crush hazard that could cause severe injury or death.
The Kroger Co is recalling HomeChef meal kits because a pretzel breading ingredient was suspect for Listeria species, though the result was not confirmed.
Randox Laboratories is recalling four kits of the Rx Series Mg Magnesium test due to reduced linearity performance.
Shimadzu Medical Systems is recalling 115 Mobile X-Ray Systems because the adjustable handle may have improper bolts, posing a risk of harm to individuals around the device.
Shimadzu is recalling 23 Trinias Digital Angiography Systems because a software defect may cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.
Shimadzu Medical Systems is recalling seven Bransist Safire Digital Angiography Systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm.
Aston Martin is recalling 151 2021 DBX vehicles because they were built without required headliner foam blocks, increasing injury risk in crashes.
TissueTech, Inc. is recalling 63 units of PROKERA non-sterile biologic corneal bandages due to potential exposure to microbial contamination.
JMH International is recalling Chef Myron's Ponzu Sauce because it contains wheat-derived ingredients despite a gluten-free claim.
GE Healthcare is recalling 5,284 MAC VU360 Electrocardiographs because they may display incorrect patient identification or demographic information.
JMH International is recalling Chef Myron's Tsukeyaki Sauce because it contains wheat-derived ingredients despite a gluten-free claim.
Randox Laboratories is recalling Randox Mg R1 kits due to reduced linearity performance, which may affect the accuracy of magnesium test results.
Shilpa Medicare Limited is voluntarily recalling 2,611 bottles of Imatinib Mesylate 100 mg tablets due to Current Good Manufacturing Practice (CGMP) deviations.
Chromsystems is recalling 3PLUS1 Multilevel Plasma Calibrator Sets because they do not meet stability criteria, which may impact test results.
Integra LifeSciences Corp. is recalling 552 instruction manuals for the Mayfield A2000 Skull Cap to correct inaccurate illustrations.
Becton, Dickinson and Company is recalling 619 vials of BD Multi-Check CD4 Low Control due to unexpected cell populations that may cause inaccurate flow cytometry results.
Welch Allyn is recalling 1,009 ELI 380 Electrocardiographs because the internal radio can disconnect from the wireless access point.
JMH International is recalling Chef Myron's Eurasian Fusion Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.
Canon Medical System is recalling 60 Aquilion Prime SP CT scanners due to a software defect that may prevent automatic scans, requiring rescans and contrast reinjection.
Spacelabs Healthcare is recalling Sentinel V10.x and V11.x software because system upgrades may add or overwrite unrelated comments on existing ECG and ABP tests.
JMH International is recalling Chef Myron's Yakitori Sauce because it contains wheat-derived ingredients despite a gluten-free claim.
JMH International is recalling Chef Myron's Tangy Teriyaki Sauce because it contains wheat-derived ingredients despite a gluten-free claim.
Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 363 vials of MassChrom Amino Acid Analysis Plasma Control Level II due to a Class II device defect.
Novocol Pharmaceutical is recalling 15,398 cartridges of Scandonest 3% Plain (Mepivacaine Hydrochloride) due to a label mix-up. The product is distributed nationwide.