State

Illinois product recalls

73,584 recalls have nationwide distribution and so reach Illinois. 11,652 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total: 11,652
Critical: 2,046
Severe: 3,022
Most recent: 2026-10-24

Of the 11,652 recalls naming Illinois we have scored against our rubric, 2,046 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,022 (26%) are Severe.

Which agencies issued them

These figures cover only the 11,652 recalls whose distribution notice names Illinois specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

451–475 of 85236

HighFDA (Devices)·Z-3254-2026·2026-09-30
Cardinal Health Recalls Presource Convenience Kits Due to Potential Seal Defects
Cardinal Health is recalling 17,503 Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Product
Presource Convenience Kits: 1) KIT, PRE OP , Catalog Number: AMN548616A; 2) KIT, NICU ADMIT NEW HAN , Catalog Number: BA1DH0116B; 3) KIT, PRE PROCEDURE , Catalog Number: IVSJV8302E; 4) KIT, IV SUPPLIES , Catalog Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3246-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recalled for Ceramic Tip Detachment Risk
Olympus is recalling 2,142 BiCOAG Hemostasis Probes because a manufacturing error may cause the ceramic tip to detach.
Product
Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V629000·2026-09-30
Greenpower Recalls EV Star Buses Due to Software Error
Greenpower is recalling 94 EV Star buses because a software error may allow the vehicle to move while the wheelchair lift is deployed.
Product
GREENPOWER — GREENPOWER EV STAR MOBILITY PLUS BUS, EV STAR BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3218-2026·2026-09-30
Midmark IQvitals Zone Recalled for Inaccurate Blood Pressure Readings
Midmark Corporation is recalling 153 IQvitals Zone units because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
Product
Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-03300 with Kit Number: 4-000-0624
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3226-2026·2026-09-30
SeaSpine Mariner Deformity Spinal Device Recall Due to Thread Depth Issue
SeaSpine Orthopedics is recalling 270 units of the Mariner Deformity Extended Polyaxial Head because the proximal thread depth is out of design specification.
Product
SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3258-2026·2026-09-30
Intervascular Recalls Cardioroot Woven Collagen Coated Vascular Grafts
Intervascular is recalling Cardioroot Woven Collagen Coated Vascular Grafts because the product failed to meet acceptance criteria for Integral Water Permeability.
Product
Cardioroot Woven Collagen Coated Vascular Graft; Model Numbers: 1. HEWROOT0024, 2. HEWROOT0026, 3. HEWROOT0028, 4. HEWROOT0030, 5. HEWROOT0032, 6. HEWROOT0034;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1392-2026·2026-09-30
United Sugar Recalls Powdered Sugar Due to Potential Wheat Kernel Contamination
United Sugar Producers and Refiners is recalling specific batches of powdered sugar due to potential wheat kernel contamination. The product was distributed in eight states.
Product
Powdered Sugar, Packaged in the following configurations: 1. United 6X, Net Wt. 50 lbs. (22.68kg), Item Number 810087. UPC 7 85921-07090 4. Distributed by: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Crystal Sugar, Net Wt. 25 lbs. (11.3 kg), Item…
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-3267-2026·2026-09-30
Medline Craniotomy Kits Recalled for Potential Endotoxin Variability
Medline is recalling 486 craniotomy convenience kits due to potential endotoxin variability that may cause adverse health reactions.
Product
Medline Convenience Kits: 1) MFC CRANIOTOMY PACK, Catalog Number: DYNJT8784; 2) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348Q; 3) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348R; 4) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348S; 5) SLUH CRANIOTOMY…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3217-2026·2026-09-30
Midmark IQvitals Zone Recalled for Inaccurate Blood Pressure Readings
Midmark Corporation is recalling IQvitals Zone devices because a performance issue may cause inaccurate blood pressure readings when using the Linear Deflation Method.
Product
Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-0320 with Kit Number: 4-000-0622
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3265-2026·2026-09-30
Medline Neurological Sponges Recalled for Potential Endotoxin Variability
Medline is recalling 695 convenience kits containing neurological sponges due to potential endotoxin variability that may cause adverse health reactions.
Product
Medline Convenience Kits: 1) PEDS SINUS PACK, Catalog Number: DYNJ02516G; 2) SINUS PACK-LF, Catalog Number: DYNJ0342705J; 3) NASAL-LF, Catalog Number: DYNJ40094G; 4) ENT PACK, Catalog Number: DYNJ50699F; 5) EENT PACK, Catalog Number: DYNJ83219
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0868-2026·2026-09-30
Amneal Recalls Exenatide Injection Pens Due to Potential Empty Delivery System
Amneal Pharmaceuticals is recalling 5,694 Exenatide Injection pens because the delivery system may be defective, potentially leaving the pen empty of medication.
Product
EXENATIDE — EXENATIDE (EXENATIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3269-2026·2026-09-30
Medline Neurological Surgery Kits Recalled for Endotoxin Variability
Medline Industries is recalling 4,013 neurological surgery kits due to potential endotoxin variability that may cause adverse health reactions.
Product
Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog Number: DYNJVB91001; 3) CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348O; 4) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348P; 5) LAMINECTOMY PACK-LF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3255-2026·2026-09-30
Cardinal Health Recalls Presource Convenience Kits Due to Seal Defects
Cardinal Health 200, LLC is recalling Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Product
Presource Convenience Kits: 1) KIT, USGPIV , Catalog Number: PVMHIVMHD; 2) KIT, USGPIV , Catalog Number: PVMHIVM14; 3) KIT, USGPIV , Catalog Number: PVMHIVM15
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V626000·2026-09-30
Starcraft Super Lite Maxx Travel Trailer Recall for Water Tank Fasteners
Starcraft RV is recalling 2022-2024 Super Lite Maxx travel trailers because fasteners may fail, causing the fresh water tank to detach and create a road hazard.
Product
STARCRAFT RV TT — STARCRAFT RV TT SUPER LITE MAXX
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3232-2026·2026-09-30
Philips Achieva 1.5T MRI Systems Recalled for Software Memory Issue
Philips is recalling 387 Achieva 1.5T MRI systems worldwide because a software issue may terminate examinations if manual scan adjustments exceed system memory.
Product
Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initial system; Model Numbers (REF): 1. 781196 (Achieva 1.5T), 2. 781343 (Achieva 1.5T), 3. 781283 (Achieva 1.5T Conversion), 4. 781346 (Achieva 1.5 Conversion), 5. 781178 (Achieva 1.5T Initial System);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3223-2026·2026-09-30
Ventec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
Ventec Life Systems is recalling 25 HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Product
REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3264-2026·2026-09-30
Baxter PRO+ Mattress Recalled for UDI Labeling Error
Baxter Healthcare is recalling six PRO+ 40-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label text.
Product
PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P7924A14
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3253-2026·2026-09-30
Criticare nGenuity Patient Monitor Recalled for Capnography Setup Error
Criticare Technologies is recalling 1,007 nGenuity Patient Monitors because a setup error renders the CO2 monitoring function inoperable, potentially delaying procedures.
Product
nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT 8100EP1-ST-US, CAT 8100EP1-US, CAT 8100EP1R
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3257-2026·2026-09-30
Baxter Recalls Two VOLARA Systems Due to Potential Flow Rate Inaccuracy
Baxter Healthcare is recalling two VOLARA systems because contamination in test equipment may have affected flow rate accuracy. Affected devices were returned and confirmed to meet specifications.
Product
Brand Name: VOLARA System Product Name: VOLARA, HC, NA A Model/Catalog Number: M08594A Software Version: N/A Product Description: VOLARA, HOMECARE, NORTH AMERICA Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3256-2026·2026-09-30
DeRoyal Myocardial Probe Recall Due to Incorrect Needle Length
DeRoyal Industries is recalling Myocardial Probes that contain an 18mm needle instead of the specified 15mm needle.
Product
REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3241-2026·2026-09-30
Philips MR 5300 MRI Scanner Software Recall for Image Reconstruction Failure
Philips is recalling 611 MR 5300 MRI scanners due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
Product
MR 5300 Model Number (REF): 1. 782110, 2. 782152;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3238-2026·2026-09-30
Philips Ingenia MRI Software Recall for Memory-Related Scan Termination
Philips is recalling Ingenia 3.0T and 3.0T CX MRI systems because a software issue can terminate examinations during image reconstruction if scan parameters exceed available system memory.
Product
Ingenia 3.0T and Ingenia 3.0T CX; Model Numbers (REF): 1. 781342(3.0T), 2. 781377(3.0T), 3. 782103(3.0T), 4. 781271(3.0T CX), 5. 782105(3.0T CX);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3225-2026·2026-09-30
Fresenius CombiSet Hemodialysis Blood Tubing Set Recalled for Handling Review
Fresenius Medical Care is recalling CombiSet Hemodialysis Blood Tubing Sets to ensure treatment preparation and handling steps are performed as instructed.
Product
CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors; Model Number: 03-2522-1;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3235-2026·2026-09-30
Philips MRI Software Recall for Image Reconstruction Failure
Philips is recalling 91 MRI systems due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Product
Evolution upgrade 1.5T and Evolution upgrade 3.0T; Model Numbers (REF): 1. 782116 (1.5T), 2. 782148 (1.5T), 3. 782117 (3.0T), 4. 782143 (3.0T);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3237-2026·2026-09-30
Philips Ingenia Ambition MRI Software Recall for Memory Limit Issue
Philips is recalling 922 Ingenia Ambition MRI systems due to a software issue that can terminate examinations if system memory is exceeded.
Product
Ingenia Ambition S and Ingenia Ambition X; Model Numbers (REF): 1. 781359 (S), 2. 782108 (S), 3. 782139 (S), 4. 781356 (X), 5. 782109 (X), 6. 782138 (X);
Category
Medical Device
Distribution
Distributed nationwide