State

Illinois product recalls

73,092 recalls have nationwide distribution and so reach Illinois. 11,640 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,640
Critical: 2,049
Severe: 2,533
Most recent: 2026-09-25

Of the 11,640 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 2,533 (22%) are Severe.

Which agencies issued them

These figures cover only the 11,640 recalls whose distribution notice names Illinois specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9076–9100 of 84732

SevereFDA (Food)·F-0319-2025·2025-01-08
Napoleonas Torte recalled for undeclared allergens and food additives
Lithuanian Bakery is recalling Napoleonas Torte due to undeclared allergens (milk, soy, wheat) and undeclared additives (sulfites, yellow 5 and 6). The product was distributed at retail stores in Iowa, Illinois, Kansas, Missouri, Minnesota, Nebraska, and South Dakota.
Product
Napoleonas Torte packaged under the following sizes: 1. Small, Net Wt 1.25 lbs. (sub ingredients contain wheat, yellow #5 and #6, and sulfites not declared on final product label) 2. Medium, Net Wt 2.75 lbs. (sub ingredients contain yellow #5 and #6 not declared on final prod
Category
Food
Distribution
7 states
SevereFDA (Food)·F-0361-2025·2025-01-08
Organic Whole Carrots Recalled for Potential E. coli O121:H19 Contamination
Grimmway Farms is recalling approximately 4,057 cases of organic whole carrots distributed nationally due to potential E. coli O121:H19 contamination. No illnesses have been reported.
Product
--- Organic Whole Carrots --- Organic Clip Carrots 50 Lbs Cal-Organic Farm; Organic Clip Carrots 50 Lbs Cal-Organic RPC --- Brand --- Cal-Organic
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0359-2025·2025-01-08
Grimmway Farms Organic Baby Carrots recalled for E. coli O121 contamination
Grimmway Farms is recalling approximately 21,094 cases of Organic Baby Carrots that may be contaminated with E. coli O121:H19. The product was distributed across 38 U.S. states, Puerto Rico, and Canada, UAE, Hong Kong, and Colombia.
Product
--- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Baby Carrots 25 Lbs. Grimmway Farms --- Brand --- Grimmway Farms
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0369-2025·2025-01-08
Bacon Avocado Wrap Recalled Due to Potential Salmonella in Cucumbers
RUSS DAVIS WHOLESALE is recalling Bacon Avocado Wraps sold under Crazy Fresh and quick & easy brands due to potential Salmonella contamination in cucumbers. 491 units were distributed across 11 states.
Product
Bacon Avocado Wrap, Net Wt 9.9oz. Keep Refrigerated. UPC 7 95631-81038 7. Containing Flour Tortilla,Carrots, Lettuce, Cheddar Cheese, Cucumber, Guacamole, Bacon Bits, Ranch Dressing, Spinach, Cream Cheese. Sold under the following brands: 1. Crazy Fresh 2. quick & eas
Category
Food
Distribution
11 states
SevereFDA (Food)·F-0371-2025·2025-01-08
Kowalski's Garden Salad Recalled for Potential Salmonella Contamination
Kowalski's Garden Salad (14 oz) is recalled due to potential Salmonella contamination in cucumbers. The recall affects 206 units distributed across 11 states with use/sell by dates November 6-15, 2024.
Product
Kowalski's Garden Salad Net Wt. 14oz. Keep Refrigerated. UPC 7 95631-89335 9. Containing Lettuce, Cucumber, Tomatoes, Broccoli, Cheddar Cheese, Onion, Hard Cooked Eggs, Carrots, Roasted Sunflower Kernels.
Category
Food
Distribution
11 states
SevereFDA (Drugs)·D-0170-2025·2025-01-08
FORCE FOREVER supplement tablets recalled for undisclosed drugs
GNMart LLC is recalling FORCE FOREVER 400mg tablets nationwide after the FDA found the product contains undisclosed Diclofenac and Dexamethasone. The Class I recall affects all lots of this dietary supplement product.
Product
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0367-2025·2025-01-08
FDA Recalls Cucumbers from Russ Davis Wholesale Due to Salmonella Risk
Russ Davis Wholesale is recalling cucumbers distributed across 11 U.S. states due to potential Salmonella contamination. A total of 1,595 units are affected.
Product
Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico. 2. Peak Cucumber Item 08009, 5 LB. Product of Mexico. 3. Cucumber Super Select Item 22200, 24 count. Product of Mexico. 4. Cucumber Item 22201, 5 lb. Produ
Category
Food
Distribution
11 states
HighFDA (Food)·F-0362-2025·2025-01-08
Beef & Lamb Gyro Meal Kit Recalled for Salmonella Risk
Reser's Fine Foods is recalling Beef & Lamb Gyro Sandwich Express Meal Kits due to potential Salmonella contamination in the tzatziki sauce. The recall affects 5,271 cases distributed across 19 states.
Product
Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz. UPC 0 13454 38313 1. Each kit contains 6 Pitas, Gyro Meat, Tzatziki Sauce 3oz. cups, Fire Feta Sauce, Feta Cheese Crumbles. Packaged in clear plastic clamshell. Distributed by Fresh Creative Foods, Vista CA.
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-0779-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling custom surgical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The recall affects 1,402 units distributed in the US, Canada, and UAE.
Product
Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF, REF DYNJ0713177; 3) BURR HOLE SHUNT PACK, REF DYNJ56819D; 4) BURR HOLE SHUNT PACK, REF DYNJ56819F; 5) BURR HOLE SHUNT PACK, REF DYNJ56819G; 6) RO VP SH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2025·2025-01-08
Baxter SIGMA Spectrum Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter is recalling SIGMA Spectrum Infusion Pump (Version 6) units that were released after repair without complete flow testing. The incomplete testing poses a risk of improper device operation.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0780-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline custom procedure kits containing non-sterile Codman Surgical Patties & Strips are being recalled due to potential endotoxin contamination. The recall affects 74 units distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0777-2025·2025-01-08
Medline surgical procedure kits recalled for non-sterile supplies
Medline is recalling custom medical procedure kits containing non-sterile surgical supplies with potential endotoxin contamination. The affected kits were distributed nationwide and internationally.
Product
Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF, REF DYNJ0382559M; 2) CRANI, REF DYNJ56001B; 3) GENDER AFFIRMING SURGERY, REF DYNJ66252; 4) GENDER AFFIRMING SURGERY, REF DYNJ66252A; 5) MAJOR NEURO PACK-LF, REF DYNJ0578916X.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0368-2025·2025-01-08
Garden Salad with Dressing Recalled Due to Potential Salmonella Contamination
Russ Davis Wholesale is recalling garden salads sold under Crazy Fresh and quick & easy brands due to potential Salmonella contamination in cucumbers. Affected products have sell-by dates of November 6-16, 2024.
Product
Garden Salad w/Ranch Dressing, Net Wt 9oz. Keep Refrigerated. UPC 7 95831-81023 3. Containing Lettuce, tomatoes, cucumbers, cheddar cheese, carrots and hard cooked egg. Sold under the following brands: 1. Crazy Fresh 2. quick & easy, Ready to Enjoy
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-0771-2025·2025-01-08
Medtronic SynchroMed II and III Implantable Pumps Recalled for Software Defects
Medtronic is recalling SynchroMed II and III implantable pumps used with a clinician tablet app that has software issues in version 2.x. Approximately 319 systems were distributed worldwide.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0785-2025·2025-01-08
Medline surgical procedure kits recalled for potential endotoxin contamination
Medline is recalling three custom surgical procedure kits due to non-sterile Codman Surgical Patties and Strips that pose a potential endotoxin contamination risk. The affected kits were distributed in the US, Canada, and the UAE.
Product
Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK, REF DYNJ66449.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0799-2025·2025-01-08
Surgical spears recalled for potential sterile barrier defect
Carwild Corporation recalls 300 Ivalon cellulose surgical spears (Model Q604237) due to potential package seal defects that could compromise sterility during ophthalmic surgical procedures.
Product
Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic Surgical Procedures For Fluid Management Model Number: Q604237
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-0778-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk
Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0772-2025·2025-01-08
SynchroMed II and III implantable pumps recalled for software issues
Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0174-2025·2025-01-08
Injectable phenylephrine recalled due to defective tamper-evident seals nationwide
Hikma Injectables is recalling phenylephrine injections nationwide because tamper-evident seals on some syringes were not properly attached. Affected lot 243120003D has a use-by date of 03/11/2025.
Product
phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0791-2025·2025-01-08
Medline Deep Brain Stimulation Surgical Kits Recalled for Non-Sterile Contamination
Medline has recalled 128 Deep Brain Stimulation surgical kits for containing non-sterile Surgical Patties and Strips with potential endotoxin contamination. Affected units were distributed worldwide including the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0773-2025·2025-01-08
Medtronic Implantable Drug Pumps Recalled for Software Defects
Medtronic has recalled 566 SynchroMed II and III implantable drug infusion pumps due to software issues in the controlling application. No injuries or illnesses have been reported.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0800-2025·2025-01-08
Surgical Nasal Packing Devices Recalled for Sterile Barrier Defect
Carwild is recalling Ivalon Anatomical Nasal Packing devices because the package seal may be defective, leaving the sterile barrier unable to be guaranteed. Lot 24F1638 with approximately 140 units was distributed across multiple U.S. states and internationally.
Product
Ivalon Anatomical Nasal Packing with Airway Tube and String, 8.0 cm x 1.5cmx 3.0 cm- Intended To Be Used During Ophthalmic Surgical Procedures For Fluid Management Model Number: Q770410
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-0781-2025·2025-01-08
Medline Nasal Pack Procedure Kits Recalled for Potential Endotoxin Contamination
Medline custom nasal pack procedure kits contain non-sterile surgical components with potential endotoxin contamination. Customers should discontinue use and contact Medline.
Product
Medline custom medical procedure kits labeled as: 1) NASAL PACK, REF DYNJ67789A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0365-2025·2025-01-08
Sam's Club Hatch Chile Chicken Enchiladas Recalled for Listeria
Sam's Club is recalling Member's Mark Hatch Chile Chicken Enchiladas because the product may contain Listeria monocytogenes.
Product
Member's Mark Hatch Chile Chicken Enchiladas, ready to cook, perishable, packaging type: aluminum/black oven-safe tray Net wt. variable - average 1.52 lbs. UPC 00226529000004, UPC 00409802813793
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0787-2025·2025-01-08
Medline Surgical Procedure Kits Recalled Due to Sterility Concerns
Medline is recalling custom surgical procedure kits that contain non-sterile surgical supplies with potential for endotoxin contamination. The kits were distributed worldwide, including the United States, United Arab Emirates, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.
Category
Medical Device
Distribution
Distributed nationwide