The Recall Desk

State

Illinois product recalls

72,919 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.

Which agencies issued them

These figures cover only the 11,602 recalls whose distribution notice names Illinois specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2376–2400 of 84521

  • ModerateFDA (Devices)·Z-1839-2026·2026-04-29

    Medline ENT and Vascular Kits with Rescinded Regulatory Clearances

    Medline Industries is recalling three ENT and vascular kits (513 units nationwide) because their regulatory clearances for certain components—Control Syringes, Guidewires, and/or High-Pressure Tubing—have been rescinded.

    Product
    Medline Kits: 1) ENT PACK, Model Number: DYNJ59030B; 2) ENT, Model Number: DYNJ908586C; 3) LH 3 PORT W/O WASTEBAG, Model Number: VASC1081C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1925-2026·2026-04-29

    Flamingo Funnel Medium surgical device recall due to sterilization incompatibility

    SurgiSmoke Solutions is recalling certain lots of Flamingo Funnel Medium (Model SQ20012-02) because a non-gamma sterilization compatible drape was used during manufacturing, which could affect device safety.

    Product
    Flamingo Funnel Medium, Model Number SQ20012-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1889-2026·2026-04-29

    Medline Convenience Kits with Polycarbonate Syringes Recalled

    Medline Industries is recalling Medline Convenience Kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance.

    Product
    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes E P DRAPE PACK-LF DYNJ0373061J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1841-2026·2026-04-29

    Medline Breast Pack Kit regulatory clearance rescinded by FDA

    The FDA has rescinded the regulatory clearance for Medline's Breast Pack Kit (Model DYNJ66777D) because certain Control Syringes, Guidewires, and High-Pressure Tubing components no longer meet regulatory standards.

    Product
    Medline Kits: 1) BREAST PACK, Model Number: DYNJ66777D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1835-2026·2026-04-29

    Medline Catheterization and Angiography Kits Regulatory Clearance Rescinded

    Medline Industries has had its 510(k) regulatory clearances rescinded for certain Control Syringes, Guidewires, and High-Pressure Tubing used in a large number of catheterization and angiography kits. The kits are distributed nationwide.

    Product
    Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF, Model Number: DYNJT2164M; 4) ANGIOGRAPHY TRAY, Model Number: DYNJT3078; 5) CATH PACK, Model Number: DYNJT4190; 6) ANGIO VASCULAR PACK, Model Number: DYNJT57
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1829-2026·2026-04-29

    Medline Namic Guidewires Recall Due to Rescinded FDA Clearance

    Medline Industries has issued a recall of Medline Namic Guidewires because their FDA 510(k) regulatory clearances have been rescinded. The affected units were distributed nationwide.

    Product
    Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJHWIRE105; 3) GWIRE HYDRO 0.035 260CM ANG S, Model Number: DYNJHWIRE107; 4) GWIRE HYDRO 0.035 260CM STR S, Model Number: DYNJHWIRE115;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1901-2026·2026-04-29

    OER-ELITE Endoscope Reprocessor Connecting Tubes Lock Lever Failure

    Olympus is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2113) because the Version 2 reprocessor connecting tube lock levers may fail prematurely. The defect could affect proper connection during endoscope reprocessing.

    Product
    OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1882-2026·2026-04-29

    Medline Polycarbonate Colored Syringes Kits Recalled for Unapproved Design Changes

    Medline Industries is recalling Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA clearance. The recall affects 270,311 units distributed nationwide and internationally.

    Product
    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes FACE/RHINOPLASTY PACK DYNJ80343C PLASTIC HEAD-NECK PACK DYNJ86639
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1849-2026·2026-04-29

    Medline Medical Device Kits Recall for Loss of 510(k) Clearance

    Medline Industries is recalling certain surgical and medical kits because their 510(k) regulatory clearances for Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. About 2,609 units were distributed nationwide.

    Product
    Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF, Model Number: DYNJ32841F; 2) CRANIOTOMY PACK-LF, Model Number: DYNJ46069D 3) CAMPUS EXTREMITY PK, Model Number: DYNJ51935A 4) FOOT -XRAY BOWL MEDCUP SPECCUP, Model Number: DYNJ68902A 5) RADIOLOGY SPINE PACK, Model Number: DYNJ806
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0490-2026·2026-04-29

    Monsel's Solution ferric subsulfate vials recalled for incorrect expiration date printing

    Premier Dental Products is recalling Monsel's Solution (ferric subsulfate) 8 mL vials because the expiration date on the vial itself is printed with an extra digit (2709114 instead of 270914). The carton expiration date is correct.

    Product
    MONSELS SOLUTION — MONSELS SOLUTION (FERRIC SUBSULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V268000·2026-04-28

    Ford Ranger and Bronco front seat pivot bolts may dislodge

    Ford is recalling certain 2024-2026 Ranger and Bronco vehicles because the front seat frame height-adjust pivot bolt may be loose or dislodged. 179,698 vehicles are affected.

    Product
    FORD — FORD BRONCO, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V269000·2026-04-28

    Lode-King Recalls Trailers With Missing Rear Impact Guard Welds

    Lode-King is recalling 2019-2026 trailers because missing welds on the rear impact guard reduce structural strength, increasing injury risk in rear-end crashes.

    Product
    LODE KING — LODE KING SDG53-3, SDF53-3, SDF50-3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V270000·2026-04-28

    Harley-Davidson motorcycles recalled for blocked breather port

    Harley-Davidson is recalling certain 2024–2026 motorcycles with a potentially blocked airbox breather port that may cause crankcase pressure to build up, risking oil ejection and injury when the dipstick is removed.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLTRXL, FXBR, FLFB, FLHLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V267000·2026-04-28

    Jayco Recalls 2026 Motorhomes Due to Missing Water Heater Valve

    Jayco is recalling 2026 Entegra Condor and Granite Ridge motorhomes because a tempering mixing valve may be missing from the water heater, creating a scalding risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, GRANITE RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V266000·2026-04-24

    Audi Q5 front seat belts may fail to restrain occupants

    Audi is recalling certain 2025 Q5, Q5 Sportback, SQ5 and SQ5 Sportback vehicles because the driver and front passenger seat belts may have been manufactured incorrectly.

    Product
    AUDI — AUDI Q5, Q5 SPORTBACK, SQ5, SQ5 SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26435·2026-04-23

    32 Degrees heated socks have caused first- and second-degree burns

    32 Degrees heated socks sold at Costco are recalled after 14 heat-related incidents, 13 of them involving first- or second-degree burns. About 207,806 units are affected.

    Product
    32 Degrees Heated Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V261000·2026-04-23

    Mack Trucks Recalls 2025-2027 Pioneer and Anthem Models for Brake Defect

    Mack Trucks is recalling 2,772 Pioneer and Anthem vehicles because unprotected electrical connectors may cause a loss of anti-lock brakes and stability control.

    Product
    MACK — MACK PIONEER PR (4), ANTHEM AN (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26431·2026-04-23

    FitRx adjustable dumbbell weight plates can dislodge from the handle

    FitRx SmartBell Quick-Select adjustable dumbbells are recalled after more than 115 reports of weight plates dislodging during use, with at least six injuries including broken toes.

    Product
    FitRx SmartBell Quick-Select 5-52.5lbs Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V264000·2026-04-23

    REV Recalls 2026 Motorhomes Due to Unexpected Generator Activation

    REV is recalling 2026 Fleetwood and Holiday Rambler motorhomes because a furnace defect may turn on the generator unexpectedly, posing a carbon monoxide risk.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FORTIS, VACATIONER, ADMIRAL, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26438·2026-04-23

    Cpzzkq baby lounger padding can obstruct an infant's breathing

    Cpzzkq baby loungers are recalled because they violate the mandatory safety standard for infant support cushions and the padding can obstruct an infant's breathing.

    Product
    Cpzzkq Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E025000·2026-04-23

    GM Recalls ACDelco Brake Fluid Due to Sediment Contamination

    General Motors is recalling specific lots of ACDelco GMW DOT 3 brake fluid that may contain visible sediment, potentially reducing brake performance.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V262000·2026-04-23

    Jeep Wagoneer S and Dodge Charger instrument panel displays may fail

    Chrysler is recalling certain Jeep Wagoneer S and Dodge Charger electric vehicles because a software error may cause the instrument panel display to fail, breaching five federal standards.

    Product
    DODGE — DODGE, JEEP CHARGER EV, WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide