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.

6601–6625 of 84590

SevereFDA (Drugs)·D-0499-2025·2025-07-09
Bupivacaine HCL Sterile Injection Recalled for Sterility Assurance Concerns
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Product
BUPIVAcaine HCL Sterile injection, USP w/EPINEPHRINE 1:200,000, 50 mg/10mL, 0.5%, (5mg/mL), 10 mL Sterile Single-Dose Vial, Rx Only, For Nerve Block, Caudal & Epidural Anesthesia Only, Warning: Contains Sulfites, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0503-2025·2025-07-09
Lidocaine HCL Sterile Injection recalled for sterility assurance concerns
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
Product
LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0001-0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2041-2025·2025-07-09
HardyCHROM CRE Culture Medium Recalled for Quality Control Failure
Hardy Diagnostics is recalling HardyCHROM CRE culture medium (Catalog No. G323) distributed across 22 US states and Puerto Rico. The product failed quality control testing due to breakthrough growth of Klebsiella pneumoniae.
Product
HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No. G323
Category
Medical Device
Distribution
22 states
SevereFDA (Devices)·Z-2037-2025·2025-07-09
BiPAP A40 ventilators are not indicated for respiratory failure patients
The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.
Product
BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2048-2025·2025-07-09
Philips Ultrasound Transducers Recalled After Over-Refurbishment
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Product
Philips 3D9-3v Transducer.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2013-2025·2025-07-09
Servo-u ventilators may measure patient circuit compliance inaccurately
The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.
Product
Servo-u Ventilator System. Model Number: 6688600.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0208-2025·2025-07-09
Bibimbap Bowl recalled due to potential Salmonella contamination
JFE Franchising Inc is recalling 13 oz Bibimbap Bowls (UPC 63912389259) because cucumbers in the product have the potential to be contaminated with Salmonella.
Product
Bibimbap Bowl 13 oz 63912389259
Category
Food
Distribution
7 states
SevereFDA (Food)·H-0206-2025·2025-07-09
Fresh cut cucumber products recalled over potential Salmonella contamination
Fresh cut cucumber products from JFE Franchising, including cucumber with ranch and cucumber with Tajin, are being recalled because the cucumbers may be contaminated with Salmonella.
Product
Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912388053 Cucumber Slices w/Tajin - 15 oz 63912388022 Cucumber Bowl w/ Ranch Dressing - 15 oz 63912388063
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0570-2025·2025-07-09
Buffered penicillin G potassium vials may actually contain cefazolin for injection
Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.
Product
PENICILLIN G POTASSIUM — PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2036-2025·2025-07-09
BiPAP A30 and BiPAP Hybrid A30 Ventilators Recalled by Philips
Philips Respironics is recalling BiPAP A30 and BiPAP Hybrid A30 ventilators. The devices do not have an indication for use in patients with respiratory failure.
Product
BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A30 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2014-2025·2025-07-09
Servo-n ventilators may measure patient circuit compliance inaccurately
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
Product
Servo-n Ventilator System. Model Number: 6694800.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2035-2025·2025-07-09
BiPAP V30 Auto ventilators are not indicated for respiratory failure
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Product
BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0210-2025·2025-07-09
Brown shell eggs recalled over potential Salmonella contamination across nine states
Brown shell eggs sold under numerous retail brands are being recalled because of potential contamination with Salmonella. The action covers 20,400,000 eggs, or 1,700,000 dozen.
Product
--- Shell Eggs; Brown; Various sizes - medium, large, and jumbo; Various pack sizes - 5, 12, 18, and Loose ---- Clover Organic Large Brown 12 eggs --- First Street Cage Free Large Brown Loose (1 case = 150 eggs) --- Nulaid Medium Brown Cage Free 12 eggs --- Nulaid Jumbo Brow
Category
Food
Distribution
9 states
HighFDA (Food)·H-0212-2025·2025-07-09
Vita Warehouse Vitamin B12 Gummies Recalled for Undeclared Peanut
Vita Warehouse Corp. is recalling four Vitamin B12 gummy products nationwide due to undeclared peanut allergen. Consumers with peanut allergies should not use the affected products.
Product
1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vitamin B12 Extra Strength Gummies 140 count 3. Vita Labs Vitamin B-12 Gummies Bulk 500 count
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2074-2025·2025-07-09
BD Heyman Follower Straight Tip catheters with incorrect French size packaging
C.R. Bard Inc is recalling BD Heyman Follower Straight Tip catheters because packaging may contain an incorrect French size designation, which could lead to use of the wrong catheter size.
Product
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2051-2025·2025-07-09
Philips C9-5EC Ultrasound Transducer Devices Recalled
Philips Ultrasound, Inc. is recalling Philips C9-5EC transducer devices that were refurbished beyond their useful life, which may affect device performance and safety.
Product
Philips C9-5EC Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2069-2025·2025-07-09
Apex Knee System components recalled over loss of sterile packaging integrity
Apex Knee System components are being recalled because the age of the nylon packaging material has caused a loss of integrity of some pouches. 341 units are affected.
Product
Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V450000·2025-07-09
Airstream Recalls 2025-2026 Interstate Motorhomes Due to Awning Lock Failure
Airstream is recalling 2025-2026 Interstate motorhomes because a module may fail to lock controls, allowing the awning to extend during transit and become a road hazard.
Product
AIRSTREAM — AIRSTREAM INTERSTATE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0500-2025·2025-07-09
Compounded ketamine injection recalled over lack of sterility assurance concerns
Ketamine Hydrochloride Injection compounded by Medivant Healthcare is being recalled for lack of assurance of sterility after an FDA inspection raised concerns about the sterile manufacturing process.
Product
KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. Kyrene Rd. Chandler, AZ 85226, NDC 81483-0006-0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2043-2025·2025-07-09
Medline IV Catheters Recalled for Needle Retraction Failure
Medline Industries is recalling specific Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters because the needle may be slow to retract or fail to retract during catheter insertion.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, REF ACC010256; 3) PEDI EMERGENCY TRAY-BLUE, REF ACC010316A; 4) ADULT DRAWER 4, REF ACC010389C;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2025·2025-07-09
Bard Urologist's Tray Recalled Over Incorrect French Size Labeling
C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.
Product
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0502-2025·2025-07-09
Compounded lidocaine with epinephrine vials lack assurance of sterility
Lidocaine HCl Sterile Injection 1% with epinephrine 1:100,000, compounded by Medivant Healthcare, is being recalled for lack of assurance of sterility. 2,825 vials affected.
Product
LIDOcaine HCL Sterile Injection, USP, 100mg/10mL, 1%, (10mg/mL), w/EPINEPHRINE 1:100,000, For Infiltration & Nerve Block, Including Caudal & Epidural Use, 10 mL Sterile Single-Dose Vial, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0211-2025·2025-07-09
Meijer dark chocolate almonds recalled for undeclared cashews in packaging
Frederik's by Meijer Dark Chocolate Almonds are being recalled because of undeclared cashews. 3,301 cases are affected across six states.
Product
Frederik's by Meijer Dark Chocolate Almonds 12 oz. resealable bag, UPC 7 08820 68730 1, 6 retail units per wholesale case. Frederik's by Meijer Dark Chocolate Almond 12 oz. box of 8, 1.5 oz. individual serving pouches, UPC 7 19283 11923 0, 6 retail units per wholesale case.
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-2045-2025·2025-07-09
Medline retinal packs recalled because catheter needle may fail to retract
Medline RETINAL PACK-LF convenience kits are being recalled because the BD Insyte Autoguard catheter needle inside may be slow to retract or fail to retract during insertion. 80 units affected.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: RETINAL PACK-LF, REF DYNJ0151148B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0203-2025·2025-07-09
Peak Cocktails blood orange spritz cans may overpressurize and explode
Peak Cocktails Blood Orange Spritz in 8.4 fl oz cans is being recalled because of overpressurization leading to exploding cans. 16,128 units are affected.
Product
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025
Category
Food
Distribution
50 states