The Recall Desk

State

Illinois product recalls

72,936 recalls have nationwide distribution and so reach Illinois. 11,603 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total
11,603
Critical
2,039
Severe
2,516
Most recent
2026-09-09

Of the 11,603 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.

These figures cover only the 11,603 recalls whose distribution notice names Illinois specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3326–3350 of 84539

  • HighCPSC·26272·2026-02-19

    Magnetic balls and rods sets recalled over a deadly choking hazard

    About 782 Huaker Magnetic Balls and Rods sets are being recalled because they contain small balls and are intended for children under three years of age.

    Product
    Huaker Magnetic Balls and Rods Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E008000·2026-02-19

    Prevost Recalls Exterior Driver Side Mirrors Due to Detachment Risk

    Prevost is recalling specific exterior driver side mirrors that may detach due to excessive play, posing a visibility and road hazard risk.

    Product
    VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26274·2026-02-19

    LED balloon lights recalled over easily accessible button cell batteries

    About 3,400 JJGoo LED Balloon Lights are being recalled because children can easily access the button cell batteries and the lights lack the warnings required by Reese's Law.

    Product
    JJGoo LED Balloon Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26276·2026-02-19

    Book nook decorations recalled over an accessible spare coin battery

    About 1,770 Prismatic 3D Prints Book Nooks with Lights are being recalled because the spare lithium coin battery can be easily accessed by children.

    Product
    Prismatic 3D Prints Book Nooks with Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26275·2026-02-19

    Children's footed sleepwear recalled over the flammability standard for sleepwear

    About 211,520 MCS and Lullaby Lane one-piece footed sleepwear items sold at Meijer are being recalled because they violate the mandatory flammability standard for children's sleepwear.

    Product
    Meijer one-piece footed 12-, 18-and 24-month children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1322-2026·2026-02-18

    Reprocessed electrophysiology catheters recalled over residual material particles

    Medline is recalling 48 reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters because these lots may contain small particles of residual material.

    Product
    Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 2-5-2mm 401211RH 401222RH 401223RH 401226RH 401227RH 401260RH 401261RH 401306RH 401309RH 401312RH 401430RH 40143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1323-2026·2026-02-18

    Reprocessed ViewFlex ICE catheters recalled over residual material particles

    Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0353-2026·2026-02-18

    UDENYCA syringes recalled after cartons were stored at room temperature

    McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.

    Product
    UDENYCA — UDENYCA (PEGFILGRASTIM-CBQV)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0491-2026·2026-02-18

    Mini beignets recalled over undeclared hazelnut in the filled product

    Costco Wholesale is recalling 8,073 packages of Kirkland Signature Mini Beignets filled with Caramel over undeclared hazelnut.

    Product
    Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Devices)·Z-1325-2026·2026-02-18

    Reprocessed AcuNav catheters recalled over residual material particles inside

    Medline is recalling 511 reprocessed Siemens ACUSON AcuNav diagnostic ultrasound catheters because these lots may contain small particles of residual material.

    Product
    Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1321-2026·2026-02-18

    Reprocessed Livewire catheters recalled over residual material particles

    Medline is recalling 41 reprocessed Livewire steerable diagnostic electrophysiology catheters because these lots may contain small particles of residual material.

    Product
    Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH; Livewire Steerable Electrophysiology Cath
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1319-2026·2026-02-18

    Reprocessed Webster CS catheters recalled over residual material particles

    Medline is recalling 228 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1324-2026·2026-02-18

    Reprocessed ultrasound catheters recalled over residual material particles inside

    Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Bios
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1320-2026·2026-02-18

    Reprocessed Inquiry catheters recalled over residual material particles inside

    Medline is recalling 311 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2026·2026-02-18

    Suture removal trays recalled over open swabstick applicator seals

    Medline is recalling 2,448 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0317-2026·2026-02-18

    Testosterone 18mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 146 pellets of Testosterone, 18.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 18.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1018-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0504-2026·2026-02-18

    Peanut butter and jam packs recalled over blue plastic pieces

    Ventura Foods is recalling 379 cases of Poco Pac creamy peanut butter and strawberry jam after the firm found pieces of blue plastic in a filter during production.

    Product
    CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1346-2026·2026-02-18

    Azurion 7 B12 systems recalled over tables that may move unexpectedly

    Philips is recalling 655 units of the Azurion 7 B12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2026·2026-02-18

    Vascular access kits and trays recalled over open swabstick seals

    Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0322-2026·2026-02-18

    Testosterone 87.5mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 62,581 pellets of Testosterone, 87.5 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 87.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1087-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1316-2026·2026-02-18

    IQon Spectral CT recalled over rotor fasteners that may be undertorqued

    Philips is recalling 52 IQon Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.

    Product
    IQon Spectral CT; Product Code (REF): 728332;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0324-2026·2026-02-18

    Testosterone 200mg single pellets recalled over potential metal particulate

    Asteria Health is recalling 194,336 pellets of Testosterone, 200 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 200 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1200-43.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1328-2026·2026-02-18

    Pediatric catheter securement kits recalled over open swabstick seals

    Medline is recalling 450 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.

    Product
    Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1349-2026·2026-02-18

    Azurion 7 M20 systems recalled over tables that may move unexpectedly

    Philips is recalling 5 of the Azurion 7 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.

    Product
    Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
    Category
    Medical Device
    Distribution
    Distributed nationwide