State

Illinois product recalls

72,984 recalls have nationwide distribution and so reach Illinois. 11,606 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,606
Critical: 2,039
Severe: 2,516
Most recent: 2026-09-16

Of the 11,606 recalls naming Illinois we have scored against our rubric, 2,039 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,516 (22%) are Severe.

Which agencies issued them

These figures cover only the 11,606 recalls whose distribution notice names Illinois specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7076–7100 of 84590

ModerateFDA (Devices)·Z-1884-2025·2025-06-04
Male-Female Midsection components from ELEOS Segmental Limb Salvage System
Onkos Surgical is recalling Male-Female Midsection components used in the ELEOS Segmental Limb Salvage System due to potential for breach of Tyvek seals. The recall affects 99 units distributed across 18 states.
Product
Male-Female Midsection with the following sizes and model numbers. a. Male-Female Midsection, 40mm, 1 EACH; Model Number: 25001040E b. Male-Female Midsection, 50mm, 1 EACH; Model Number: 25001050E c. Male-Female Midsection, 60mm, 1 EACH; Model Number: 25001060E d. Mal
Category
Medical Device
Distribution
18 states
ModerateFDA (Drugs)·D-0452-2025·2025-06-04
Theophylline Extended-Release Tablets recalled for dissolution test failure
Glenmark Pharmaceuticals is recalling Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, due to out-of-specification results on dissolution testing. The recall affects 8,520 bottles distributed nationwide.
Product
THEOPHYLLINE — THEOPHYLLINE (THEOPHYLLINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1882-2025·2025-06-04
Segmental Stem Bowed 152MM components recall potential seal breach
Onkos Surgical is recalling Segmental Stem, Canal Filling, Bowed 152MM components of the ELEOS Limb Salvage System due to potential breach of Tyvek seals. The defect could compromise the sterility of the device.
Product
Segmental Stem, Canal Filling, Bowed 152MM, 1 EACH. Model Numbers: FB-11152-03M, FB-12152-03M, FB-13152-03M, FB-14152-03M, FB-15152-03M, FB-16152-03M, FB-17152-03M, FB-18152-03M, FB-19152-03M, FB-20152-03M, FB-21152-03M. Component of ELEOS LIMB SALVAGE SYSTEM
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-1832-2025·2025-06-04
ORTHO CLINICAL DIAGNOSTICS VITROS Phosphorus Reagent Recall
ORTHO CLINICAL DIAGNOSTICS INC VITROS PHOSPHORUS reagent units may have been stored outside recommended cold chain conditions due to severe thunderstorms, risking incorrect or delayed test results.
Product
ORTHO CLINICAL DIAGNOSTICS INC VITROS PHOSPHORUS (60/CR 5CR/PK) ORCLNL REAGENT.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1846-2025·2025-06-04
Abbott Point of Care Creatinine Test Cartridges Recalled for Storage Failure
McKesson Medical-Surgical is recalling Abbott Point of Care Test Creatinine I-STAT cartridges distributed nationwide after transit delays during severe thunderstorms caused improper storage conditions, increasing the risk of incorrect or delayed test results.
Product
ABBOTT POINT OF CARE TEST CREA I-STAT (25/BX) ABBTPT CARTRIDGE.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1862-2025·2025-06-04
GM Helix Acqua Implant labeled 11.5 mm may contain 13 mm
Straumann USA LLC is recalling GM Helix Acqua Implants (Article Number 140.984) because packages labeled as 11.5 mm implants may contain 13 mm implants instead.
Product
GM Helix Acqua Implant, Article Number: 140.984
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1845-2025·2025-06-04
Abbott Diagnostics HIV Combo Calibrator Affected by Cold Chain Exposure
Abbott Diagnostics ARCHITECT HIV COMBO Calibrator units may have been exposed to improper storage temperatures due to transit delays during severe thunderstorms, potentially affecting test accuracy.
Product
ABBOTT DIAGNOSTICS ARCHITECT HIV COMBO 1X4ML CALIBRATOR.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1835-2025·2025-06-04
Ortho Clinical Diagnostics Total Bili-Alkp XT Reagent Recall
Mckesson Medical-Surgical is recalling Ortho Clinical Diagnostics Total Bili-Alkp XT (L-Sequester) reagent due to cold chain storage failures during transit caused by severe thunderstorms, which may result in incorrect or delayed test results.
Product
ORTHO CLINICAL DIAGNOSTICS INC TOTAL BILI-ALKP XT (L-SEQUESTER) (300/PK) REAGENT.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1880-2025·2025-06-04
Segmental Stem Components Recalled for Potential Tyvek Seal Breach
Onkos Surgical is recalling Segmental Stem components of the ELEOS Limb Salvage System due to potential breach of Tyvek seals. The defect could compromise sterility.
Product
Segmental Stem, Cemented, Bowed, 152MM, 1 EACH. Model Numbers: CB-11152-03M, CB-13152-03M, CB-15152-03M, CB-17152-03M. Component of ELEOS LIMB SALVAGE SYSTEM
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-1822-2025·2025-06-04
Siemens ADVIA Centaur HCY Calibrator packs recalled for calibrator instability
Siemens Healthcare Diagnostics is recalling certain lots of ADVIA Centaur HCY Calibrator (2 Pack) due to calibrator instability that causes increased positive bias and fails to meet reference interval specifications in the Instructions for Use.
Product
ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1825-2025·2025-06-04
Abbott Rapid DX Cholestec LDX Lipid Profile Test Cassettes Recall
Abbott Rapid DX Cholestec LDX Lipid Profile test cassettes are being recalled because transit delays caused by severe thunderstorms may have exposed products to storage temperatures outside recommended conditions, which could result in incorrect or delayed test results.
Product
ABBOTT RAPID DX N AMERICA LLC, TEST CHOLESTEC LDXLIPID PROFILE (10/BX 50BX/CS) CASSETTES.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1851-2025·2025-06-04
Abbott Diagnostics Architect Progesterone Reagent Storage Condition Recall
Abbott Diagnostics Architect Progesterone (100 tests) reagent is being recalled due to transit delays during severe thunderstorms that may have caused storage outside recommended conditions, risking incorrect or delayed test results.
Product
ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1842-2025·2025-06-04
Abbott Diagnostics ARCH AUSAB Anti-HBS Reagent Recall
Abbott Diagnostics ARCH AUSAB Anti-HBS reagent units may have been stored outside recommended temperature conditions due to transit delays caused by severe thunderstorms, potentially leading to incorrect or delayed test results.
Product
ABBOTT DIAGNOSTICS ARCH AUSAB ANTI-HBS (100/EA) REAGENT.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1859-2025·2025-06-04
Ultrasonic Cleaning Systems Triton 36 and 72 recalled
Ultra Clean Systems, Inc. is recalling Ultrasonic Cleaning Systems Triton 36 and Triton 72 models due to carbon filter sensors breaking down from electrochemical degradation. The defect was identified during routine preventative maintenance checks.
Product
Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1834-2025·2025-06-04
Ortho Clinical Diagnostics Diluent Pack Recall Due to Cold Chain Failure
McKesso Medical-Surgical Inc. is recalling Ortho Clinical Diagnostics FS Diluent Packs due to transit delays from severe thunderstorms that may have caused improper storage conditions. The affected products could produce incorrect or delayed test results.
Product
ORTHO CLINICAL DIAGNOSTICS INC FS(3PK/BX)ORCLNL DILUENT PACK 3.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1838-2025·2025-06-04
HemoCue Inc Hemotrol Low Control affected by cold chain transit delays
HemoCue Inc Hemotrol Low Level 1 control product was subject to transit delays during severe thunderstorms that may have caused storage outside recommended temperature conditions, potentially leading to incorrect or delayed test results.
Product
HEMOCUE INC HEMOTROL LOW 2X1ML LEVEL 1 HEMCUE CONTROL.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1828-2025·2025-06-04
BD Microbiology Fluid Thioglycollate Medium Tubes Recall
McKessan Medical-Surgical is recalling BD Microbiology Fluid Thioglycollate Medium tubes due to transit delays and severe thunderstorms that may have caused storage outside recommended conditions, potentially resulting in incorrect or delayed test results.
Product
BD MICROBIOLOGY FLUID THIOGLYCOLLATE MED TUBE 1004321196 (100/CT) MEDIA.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1847-2025·2025-06-04
Abbott ARCHITECT HBSAG Assay Reagent Recall Due to Storage Condition Failure
Abbott ARCHITECT HBSAG Assay reagent may have been stored outside recommended conditions due to transit delays caused by severe thunderstorms, potentially resulting in incorrect or delayed test results.
Product
ABBOTT DIAGNOSTICS ARCHITECT HBSAG ASSAY(100TST/BX) BDS REAGENT.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1830-2025·2025-06-04
Abbott HbA1c Hemoglobin Afinion Test Kit Cold Chain Failure
Abbott HbA1c Hemoglobin Afinion test kits are being recalled due to transit delays caused by severe thunderstorms that may have exposed products to storage temperatures outside the manufacturer's recommended range, potentially causing incorrect or delayed test results.
Product
ABBOTT RAPID DX N AMERICA LLC HBA1C HEMOGLOBIN AFINION GLYCTD (15TST/BX) TEST KIT.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1815-2025·2025-06-04
Apo B Reagent calibration error may produce inaccurate test results
Beckman Coulter is recalling Apo B Reagent due to an erroneous value in the calibration sheet that could generate incorrect patient test results with positive bias up to 42%.
Product
Apo B Reagent, REF: OSR6143
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V370000·2025-06-03
2022-2025 Rivian R1T and R1S recalled for unsecured seat belt anchors
Rivian is recalling certain 2022-2025 R1T and R1S vehicles. D-ring bolts for front seat belt anchorages may not have been properly installed, potentially failing to restrain occupants during a crash.
Product
RIVIAN — RIVIAN R1T, R1S
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·019-2025·2025-06-03
Sulu Organics Recalls Pork Lard and Beef Tallow Lacking Federal Inspection
Sulu Organics LLC is recalling pork lard and beef tallow products produced without federal inspection. Consumers should not consume these items.
Product
Sulu Organics LLC Recalls Pork Lard & Beef Tallow Products Produced Without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V371000·2025-06-03
2025 Ford Explorer Brake Caliper Bolts May Be Improperly Secured
Ford is recalling certain 2025 Explorer vehicles because front brake caliper bolts may not be properly secured, potentially affecting brake function. Dealers will inspect and repair the bolts at no cost.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·020-2025·2025-06-03
Springville Meat Recalls Beef Jerky for Undeclared Fish Allergen
Springville Meat & Cold Storage Co. is recalling beef jerky and snack sticks because they contain undeclared anchovies, a known fish allergen.
Product
Springville Meat & Cold Storage Co. Inc. — Springville Meat & Cold Storage Co., Inc., Recalls Beef Jerky/ Beef Snack Stick Products and Voluntarily Inspected Elk, Venison and Buffalo Jerky Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-06032025-01·2025-06-03
USDA Issues Public Health Alert for Organic Ground Beef Due to E. Coli O157:H7
USDA FSIS issued a public health alert for Organic Rancher ground beef potentially contaminated with E. coli O157:H7. Consumers are urged not to consume the product.
Product
NPC Processing, LLC — FSIS Issues Public Health Alert for Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
Distributed nationwide