The Recall Desk

State

Illinois product recalls

72,913 recalls have nationwide distribution and so reach Illinois. 11,602 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total
11,602
Critical
2,039
Severe
2,515
Most recent
2026-09-09

Of the 11,602 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 2,515 (22%) are Severe.

These figures cover only the 11,602 recalls whose distribution notice names Illinois specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2001–2025 of 84515

  • HighNHTSA·26V308000·2026-05-14

    Hyundai Elantra Hybrid power control units may overheat

    Hyundai is recalling certain 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit assembly may overheat, increasing the risk of a fire. 54,337 vehicles are affected.

    Product
    HYUNDAI — HYUNDAI ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26484·2026-05-14

    LiCB CR2032 Lithium Coin Batteries Recalled for Child-Resistant Packaging Violation

    Guangzhou Lichengbei Battery Technology Co., Ltd. (LiCB) has recalled about 94,000 CR2032 3V lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Ingestion can cause serious internal injuries, chemical burns, and death.

    Product
    LiCB CR2032 3V Lithium Coin Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·26486·2026-05-14

    Amazon Basics 55 Lbs. Adjustable Dumbbells Recalled for Impact Hazard

    Amazon is recalling Amazon Basics 55 Lbs. Adjustable Dumbbells because weight plates can fail to engage completely and dislodge during use, posing an impact hazard. No injuries have been reported.

    Product
    Amazon Basics 55 Lbs. Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1935-2026·2026-05-13

    Aurous Centimeter Sizing Catheter Recalled for Marker Band Cracking Risk

    Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.

    Product
    Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiographic procedures and available in a variety of lengths (70 and 100 cm) and tip co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1934-2026·2026-05-13

    Cook Centimeter Sizing Catheter recall due to marker band cracking

    Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.

    Product
    Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials and designs (e.g., polyethylene or nylon, non-braided or braided with 1:1 torque)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1977-2026·2026-05-13

    Halyard PERC TRAY Kit Syringe Adaptor Connection Risk Recall

    The Halyard PERC TRAY kit (models SLPC34-01 and SLPC34-02) is being recalled due to risk that a Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.

    Product
    Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1970-2026·2026-05-13

    Halyard Cardiac Cath Pack Kit Syringe Adapter Unwinding Risk

    AVID Medical recalls Halyard Cardiac Cath Pack kits (Models EAMC1000-05, WAFB208-02) due to risk that a Medline syringe rotating adapter may unwind during use, causing loose or full disconnection between the syringe and manifold.

    Product
    Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1971-2026·2026-05-13

    Halyard CARDIAC CATH PACK SAN23CARDQ Kit Syringe Adapter Risk

    AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (Model DRCC36) due to a Medline syringe rotating adapter that may unwind during use, potentially causing loose or full disconnection between the syringe and manifold.

    Product
    Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1978-2026·2026-05-13

    Halyard SAMMC Angiography Kit syringe rotating adapter unwinding recall

    Halyard SAMMC ANGIOGRAPHY kits (Model SAMM066-15) are recalled because the Medline syringe rotating adapter may unwind during use, causing a loose or disconnected connection between the syringe and manifold. 2,392 kits were distributed across US states including FL, IL, MO, MS, NC, NE, and TX.

    Product
    Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-2108-2026·2026-05-13

    Medline Labor and Delivery Kits Recalled for Sterilization Calibration Issues

    Medline Industries is recalling approximately 29,192 labor and delivery kits and OB packs due to calibration issues in sterilization equipment that may impact sterility assurance. The products were exposed to validated sterilization cycles, but the calibration problems potentially compromise sterile status.

    Product
    Medline Convenience Kits: 1) OB KIT, Model Number: DYKM2326; 2) KIT LABOR DELIVERY TUBAL LIGAT, Model Number: DYKMBNDL165; 3) KIT LABOR & DELIVERY D&C/D&E, Model Number: DYKMBNDL31; 4) KIT LABOR & DELIVERY CERCLAGE, Model Number: DYKMBNDL38; 5) KIT LABOR & DELIVERY CERCL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1973-2026·2026-05-13

    Halyard CATH LAB Kit Recalled for Syringe Adapter Disconnection Risk

    AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75AM) because the syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.

    Product
    Halyard CATH LAB kit. Model Number: SACL75AM.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Food)·H-0765-2026·2026-05-13

    Raw Farm bulk shredded cheddar linked to multistate E. coli outbreak

    Raw Farm Shredded Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.

    Product
    RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-0523-2026·2026-05-13

    Naproxen Oral Suspension Recalled for Lead and Lithium Contamination

    Acella Pharmaceuticals is recalling Naproxen oral suspension due to the presence of lead and lithium above specification levels. The recall affects 6,336 bottles distributed nationwide.

    Product
    NAPROXEN — NAPROXEN (NAPROXEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0766-2026·2026-05-13

    Raw Farm bulk raw cheddar linked to multistate E. coli outbreak

    Raw Farm Original Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.

    Product
    RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1855-2026·2026-05-13

    Intuitive 8 mm SureForm 30 Gray Reloads Incomplete Staple Defect

    Intuitive Surgical is recalling Intuitive 8 mm SureForm 30 Gray Reloads (Reference Numbers 48230M-05 and 48230M-06) because they may produce an incomplete staple line during curved-tipped stapler operations.

    Product
    Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2106-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization equipment calibration issues

    Medline Industries is recalling four Convenience Kit models (892 units) nationwide because sterilization and packaging equipment calibration issues may have compromised the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY, Model Number: DYNDA2941A; 2) CHEST/BREAST-LF, Model Number: DYNJ83950; 3) HERNIA REPAIR TOTE, Model Number: DYNJ908337A; 4) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0691-2026·2026-05-13

    Costco deli meatloaf seasoning recalled over potential Salmonella contamination

    Meatloaf seasoning packed for the Costco service deli is being recalled after the firm's supplier reported that the nonfat dry milk may be contaminated with Salmonella.

    Product
    Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags Net Weight: 20lbs Allergy Information: CONTAINS: MILK, WHEAT Packed BY: Griffith Foods STONECREST, GA 30058
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Devices)·Z-1974-2026·2026-05-13

    Halyard CATH LAB Kit Due to Syringe Adapter Disconnection Risk

    AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75-01) due to risk that a Medline syringe rotating adaptor may unwind during use, causing loose or complete disconnection between the syringe and manifold.

    Product
    Halyard CATH LAB kit. Model Number: SACL75-01.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1976-2026·2026-05-13

    Halyard NEURO IR PERIPHERAL kit syringe adapter may disconnect

    AVID Medical is recalling the Halyard NEURO IR PERIPHERAL (PS 64405) kit because the Medline syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.

    Product
    Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-2064-2026·2026-05-13

    Endoscopy Pump Tubing/Cap Set water aspiration risk recall

    Erbe Medical is recalling ERBEFLO 2 Endoscopy Pump Tubing/Cap Sets due to a connector design that may allow unintended water flow, potentially leading to water aspiration and serious respiratory conditions.

    Product
    ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0517-2026·2026-05-13

    PurPrep Povidone-Iodine and Isopropyl Alcohol Solution Recalled for Sterility Assurance

    CareFusion 213, LLC is recalling PurPrep sterile topical solution due to lack of assurance of sterility and potential product contamination. The affected product is a povidone-iodine and isopropyl alcohol solution distributed nationwide.

    Product
    PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0764-2026·2026-05-13

    Raw Farm shredded raw cheddar linked to multistate E. coli outbreak

    Raw Farm Raw Cheddar Simply Shredded Original in 8 oz packs is being recalled in connection with a multi-state outbreak of E. coli O157:H7.

    Product
    RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP REFRIGERATED INGREDIENTS: WHOLE RAW MILK, VEGETABLE RENNET, CULTURES, KOSHER SEA SALT Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 8
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1972-2026·2026-05-13

    Halyard Cardiac Catheterization Tray Kits Recalled for Connection Risk

    AVID Medical is recalling Halyard CARDIAC CATH TRAY SHANDS JAX kits due to a defect in the Medline syringe rotating adaptor that may unwind during use, causing a loose or full disconnection between the syringe and manifold.

    Product
    Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0513-2026·2026-05-13

    DELFLEX Peritoneal Dialysis Solution Recall Due to Potential Sterility Issues

    Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from bag perforations that could compromise sterility. Affected patients should contact their healthcare provider immediately.

    Product
    DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2.5% DEX. LM/LC, 2L 5PK, Part Number 054-20222, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0763-2026·2026-05-13

    Raw Farm jalapeno raw cheddar linked to multistate E. coli outbreak

    Raw Farm Raw Cheddar Jalapeno is being recalled in connection with a multi-state outbreak of E. coli O157:H7, covering the named batches and all prior batches and dates.

    Product
    RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt, 100% organic chili powder jalapeno, air dried green jalapeno peppers Produced By: RAW
    Category
    Food
    Distribution
    10 states