State
73,187 recalls have nationwide distribution and so reach Illinois. 11,643 additional recalls listed Illinois specifically in their distribution scope.
Of the 11,643 recalls naming Illinois we have scored against our rubric, 2,049 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,535 (22%) are Severe.
Which agencies issued them
These figures cover only the 11,643 recalls whose distribution notice names Illinois specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wiers Farm Inc is recalling Butternut Squash in 1-pound cartons due to potential Listeria monocytogenes contamination. Lot numbers 240705 through 240712 are affected.
Wiers Farm green bell peppers packaged in 1-pound cartons are being recalled due to potential Listeria monocytogenes contamination. Affected lot numbers are 240705 through 240712, distributed across 17 states.
Wiers Farm Inc is recalling habanero peppers sold in 1-pound cartons across 17 states due to potential Listeria monocytogenes contamination. The recall involves 441 cases with lot numbers 240705 through 240712.
Wiers Farm Inc is recalling 148 cases of Plain Parsley due to potential Listeria monocytogenes contamination. The affected product was distributed across 17 states.
Wiers Farm Inc is recalling Serrano Peppers sold in 4oz bags due to potential Listeria monocytogenes contamination. The recall affects approximately 1,708 cases distributed across 16 states.
Wiers Farm is recalling organic zucchini squash due to potential Listeria monocytogenes contamination. The recall affects 337 cases across 17 states with lot numbers 240705 through 240712.
Wiers Farm is recalling cilantro packaged in 1-pound cartons due to potential Listeria monocytogenes contamination. The affected product was distributed to 2,798 cases across 16 U.S. states.
Philips IntelliVue Patient Monitor models with software L.x and M.x lack critical monitoring capabilities due to a software update. This could result in incorrect or delayed patient treatment.
Granules Pharmaceuticals Inc. is recalling Gabapentin Tablets 600 mg nationwide after fused Metformin ER tablets were found in bottles, creating a risk of unintended medication exposure.
FDA recall of BD PYXIS MEDBANK automated medication dispensing cabinets due to a software defect that prints incorrect bin information on restock labels, potentially leading to medication identification errors.
Lipari Foods is recalling Premo King Club Footlong sandwiches (UPC 612510094259) due to potential Salmonella contamination. The recall affects 216 cases distributed to retailers across 16 states; consumers should discard the product or return it to the store.
BD PYXIS MEDBANK automated medication dispensing cabinets with software version 3.9.1.9 may generate incorrect bin location labels during restocking. This could cause medications to be placed in wrong storage locations.
Certain 2019-2025 Holiday Rambler Admiral and other RVs have exterior patio outlets lacking GFCI protection when powered by generator or shore cord, increasing electrical shock risk. Dealers will install GFCI devices free of charge.
Palmer & Company is recalling Palmer Patriotic White Fudge Cookies in 7oz and 13.5oz sizes due to potential salmonella contamination. Affected products were distributed nationwide in the United States and Canada.
The Philips Azurion Interventional Fluoroscopic X-ray System may lose imaging functionality or experience longer restart times. The FDA is recalling approximately 3,011 units of this device worldwide.
A software issue in the BD PYXIS MEDBANK automated medication dispensing cabinet can cause incorrect bin labels to be printed for restock operations. This could lead to medication administration errors affecting patient safety.
Philips IntelliVue Patient Monitors (MX400/450/500/550) with software versions L.x or M.x lack required monitoring capabilities due to removed software entitlements. The missing features could lead to incorrect or delayed patient treatment.
BioFire Diagnostics is recalling gastrointestinal diagnostic test kits due to false positive Vibrio results when used with certain transport mediums.
Steris Corporation recalls certain automated endoscope reprocessor hookups due to incorrect instructions in product documentation. Improper hookup connection could prevent proper endoscope disinfection, risking patient infection.
American Contract Systems is recalling 29 gynecological laparoscopy surgical kits due to insufficient aeration during sterilization, which may compromise sterility and increase infection risk for patients.
CareFusion's BD PYXIS MEDBANK medication dispensing cabinets (software 3.9.1.9) have a software defect that may cause restock labels to print incorrect medication bin locations, creating a risk of medication dispensing errors.
Nuts.com is recalling Ground Sumac products due to undeclared gluten. Products were distributed online to consumers in multiple U.S. states, Canada, and the U.S. Virgin Islands.
Siemens LUMINOS Lotus Max X-ray displays are being recalled because the support arm may lower unintentionally, potentially injuring people nearby during positioning.
The support arm on Siemens Multitom Rax X-ray systems may unintentionally lower, creating a fall risk to people positioned beneath the ceiling-mounted display during system positioning.
Steris Hookup Model 2-8-540 instructions were incorrectly documented, potentially preventing proper endoscope disinfection and risking patient infection.