The Recall Desk

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.

426–450 of 85236

  • SevereFDA (Drugs)·D-0861-2026·2026-09-30

    Sterling Recalls Major LubriFresh P.M. Ointment for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling Major LubriFresh P.M. Nighttime Ointment due to a lack of assurance of sterility. The recall covers 34,368 tubes distributed nationwide.

    Product
    Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1391-2026·2026-09-30

    United and Good & Gather Light Brown Sugar Recalled for Wheat Contamination

    United Sugar Producers and Refiners is recalling specific batches of United and Good & Gather light brown sugar due to potential wheat kernel contamination.

    Product
    Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051. Distributed By: United Sugar Producers & Refiners, Minneapolis, MN 55439. 2. Good & Gather, Net Wt 2 lb. (32 oz) 907g. Item Number 817773. UPC 0…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0863-2026·2026-09-30

    AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution due to a lack of assurance of sterility.

    Product
    CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3266-2026·2026-09-30

    Medline Neurological Sponges Recalled for Potential Endotoxin Variability

    Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.

    Product
    Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DYNJ81325A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3244-2026·2026-09-30

    Olympus BiCOAG Hemostasis Probe Recall Due to Ceramic Tip Detachment Risk

    Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.

    Product
    Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0855-2026·2026-09-30

    AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% due to a lack of assurance of sterility.

    Product
    CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0870-2026·2026-09-30

    Clear Eyes Redness Relief Eye Drops Recalled for Sterility Concerns

    Insight Pharmaceuticals is recalling 2.3 million bottles of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.

    Product
    Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0871-2026·2026-09-30

    Clear Eyes Redness Relief Eye Drops Recalled for Sterility Assurance Issues

    Insight Pharmaceuticals is recalling specific lots of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.

    Product
    Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0857-2026·2026-09-30

    Walgreens Lubricant Eye Drops Recalled for Lack of Sterility Assurance

    Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. Consumers should stop using the product.

    Product
    WALGREENS LUBRICANT EYE DROPS — WALGREENS LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3214-2026·2026-09-30

    Boston Scientific Recalls Imager II Angiographic Catheters Due to Tip Fracture Risk

    Boston Scientific is recalling Imager II Angiographic Catheters because the tip may fracture or detach, potentially causing device fragments to remain in or migrate through the patient's vasculature.

    Product
    Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5; M001314021 IMAGER II/5/ST/65/035 BX 5; M001314031 IMAGER II/5/ST/100/035 BX 5; M001314041 IMAGER II/5/BARNH/100/038 BX5; M001314051 IMAGER…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3140-2026·2026-09-30

    CooperSurgical Recalls Neonatal Nasal CPAP Replacement Sets Due to Loose Tubing

    CooperSurgical is recalling 149 boxes of INCA Neonatal Nasal CPAP replacement sets because the flexible tubing may disconnect from the nasal cannula, potentially reducing treatment effectiveness.

    Product
    INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-0712, 44-0707, 44-0709, 44-0715.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3229-2026·2026-09-30

    Medline Instrument Channel Brush Kits Recalled for Sharp Edges

    Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.

    Product
    Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3245-2026·2026-09-30

    Olympus BiCOAG Hemostasis Probe Recalled for Ceramic Tip Detachment Risk

    Olympus is recalling 105 BiCOAG Hemostasis Probes because a manufacturing defect may cause the ceramic tip to detach during use.

    Product
    Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector. Model/Catalog Number: CD-B612LA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3247-2026·2026-09-30

    Olympus BiCOAG Hemostasis Probe Recalled for Potential Ceramic Tip Detachment

    Olympus Corporation of the Americas is recalling 816 units of BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.

    Product
    Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3249-2026·2026-09-30

    Philips EPIQ Elite Ultrasound System Recalled for Software Error

    Philips is recalling 219 EPIQ Elite Diagnostic Ultrasound Systems due to a software issue that may cause inaccurate blood flow velocity measurements and potential misdiagnosis.

    Product
    Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3250-2026·2026-09-30

    Becton, Dickinson ForeSight Elite Tissue Oximetry Cable Recall for Incorrect Channel Switching

    Becton, Dickinson and Company is recalling 15,455 ForeSight Elite Tissue Oximetry Cables due to incorrect switching of Channel 1 and 2 on the module and flag labels.

    Product
    ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter cable is intended for use as an adjunct monitor of absolute regional hemoglobin oxygen saturation of blood under the sensors in individuals at risk for reduced…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3215-2026·2026-09-30

    Heidelberg SPECTRALIS Flex Module Recall Due to Wheel Detachment Risk

    Heidelberg Engineering is recalling 87 SPECTRALIS units with Flex Modules because wheels may detach, causing the stand to tip over and injure nearby people.

    Product
    Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module Model/Catalog Number: S3610, S2610, S2000, S1610 multimodal imaging platform optimized for the posterior segment of the eye
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3224-2026·2026-09-30

    Maquet PowerLED 300 Concealed Lighting System Recalled for Detachment Risk

    Maquet is recalling 667 PowerLED 300 Concealed Lighting Systems because the spring arm may detach and fall, posing a potential injury risk.

    Product
    PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3251-2026·2026-09-30

    Abiomed Recalls Automated Impella Controllers Due to Firmware and Software Defects

    Abiomed is recalling 3,322 Automated Impella Controllers worldwide due to firmware and software defects that affect pressure signal accuracy and system reliability.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3230-2026·2026-09-30

    Medline Instrument Channel Brush Kits Recalled for Sharp Edges

    Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.

    Product
    Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3219-2026·2026-09-30

    Midmark IQvitals Zone Recalled for Inaccurate Blood Pressure Readings

    Midmark Corporation is recalling 20 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: 1-200-0350 with Kit Number: 4-000-0722
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3268-2026·2026-09-30

    Medline Neurological Surgery Kits Recalled for Endotoxin Variability

    Medline is recalling 234 neurological surgery kits nationwide due to potential endotoxin variability that may cause adverse health reactions.

    Product
    Medline Convenience Kits: 1) MAJOR NEURO VCH, Catalog Number: DYNJ39218I; 2) NEURO PACK-LF, Catalog Number: DYNJ41246F; 3) CRANIOTOMY PACK (CRSJE)227-LF, Catalog Number: DYNJ47487A; 4) MAJOR NEURO PACK, Catalog Number: DYNJ57233J; 5) NEURO, Catalog Number: DYNJ82388A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3220-2026·2026-09-30

    Midmark IQvitals Zone Recalled for Inaccurate Blood Pressure Readings

    Midmark Corporation is recalling 33 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: 1-200-0360 with Kit Number: 4-000-0724
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3259-2026·2026-09-30

    New York Embroidery Studio Recalls Isolation Gowns for Liquid Barrier Failure

    New York Embroidery Studio is recalling 5,400 Trinity Non-Surgical Isolation Gowns because they do not consistently meet minimum liquid-barrier performance requirements.

    Product
    New York Embroidery Studio Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large. Model Number: NYES100-2. Packaged in inner packs of 10 and 100 gowns per shipping case.
    Category
    Medical Device
    Distribution
    Distributed nationwide