State

Illinois product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1276–1300 of 84509

HighFDA (Devices)·Z-2493-2026·2026-06-24
Medline procedure kits contain catheters failing performance specifications
Medline medical procedure kits including ECMO chest exploration, coronary artery bypass and D&C/cysto trays are being recalled because sample catheters did not meet performance specifications.
Product
MEDLINE Medical Procedure Kits labeled as: 1) CHEST EXPLORATION ECMO, Medline Kit Number/SKU DYNJ63789A; 2) CORONARY/ARTERY BYPASS TRAY, Medline Kit Number/SKU DYNJ17321G; 3) D&C/CYSTO, Medline Kit Number/SKU DYNJ909989B; 4) DDD LAPAROSCOPY PACK, Medline Kit Number/SKU D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2517-2026·2026-06-24
Splashwire hydrophilic guide wire pouches have unsealed portions
Merit Medical Splashwire Hydrophilic Guide Wires are being recalled because of unsealed portions of pouches. 5,004 units are affected.
Product
Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF: MSWSTDA35180 UDI-DI codes: 00884450529645 00884450529669 REF: MSWSTDA35260EX UDI-DI code: 00884450529683 REF: MSWSTDA3580 UDI-DI codes: 008844
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2484-2026·2026-06-24
Medline coude latex catheters fail applicable performance specifications
Medline Intermittent Latex Coude Catheters pre-connected to a collection bag, 16 Fr, are being recalled across all lots because samples did not meet performance specifications. 10,980 units affected.
Product
MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 16 Fr, 1000mL, Medline Product Number/SKU (REF) URO4RR16C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2475-2026·2026-06-24
Giraffe OmniBed incubator canopy fasteners can fall into patient compartment
Giraffe OmniBed incubator-warmers, all models, are being recalled because fasteners securing the canopy soffit can disengage and fall into the patient compartment. 19,587 units affected.
Product
Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2513-2026·2026-06-24
iLet Bionic Pancreas pumps may become stuck on the lock screen
The iLet Bionic Pancreas is being recalled because a screen unlock failure can leave the user stuck on the Lock Screen, unable to change the cartridge or announce a meal.
Product
iLet Bionic Pancreas, REF: BB1001
Category
Medical Device
Distribution
51 states
HighFDA (Devices)·Z-2509-2026·2026-06-24
STAAR ICL calculation software miscalculates toric lens orientation diagram printout
STAAR ICL Calculation Software version 8.00 is being recalled because of a coding issue in calculating the implantation orientation diagram printout for toric implantable collamer lenses.
Product
Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL Calculation Software is designed as an aide in the calculation of the size and diopter power (with residual refraction) for physician selection of the lens. For toric
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2448-2026·2026-06-24
HarmonyAIR A-Series surgical light heads may show paint delamination
HarmonyAIR A-Series Surgical Lighting Systems are being recalled because of the potential for paint delamination, meaning chipping or peeling, on the light heads. 4,138 units affected.
Product
HarmonyAIR A-Series Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0640-2026·2026-06-24
Med Pride hydrocortisone cream 1oz tubes recalled over manufacturing deviations
Med Pride Hydrocortisone Cream 1%, 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,944 tubes are affected.
Product
Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 1 oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30503 0.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0590-2026·2026-06-24
Kerr Insta-Char aqueous charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char in an aqueous base, 50 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0591-2026·2026-06-24
Kerr Insta-Char activated charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char activated charcoal in a sorbitol base with cherry flavor is being recalled because the product did not meet the Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0602-2026·2026-06-24
DHP benzocaine topical anesthetic gel bottles may have incomplete seals
DHP Topical Anesthetic Gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units are affected.
Product
HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0630-2026·2026-06-24
Lucky Super Soft triple antibiotic ointment recalled over manufacturing deviations
Lucky Super Soft First Aid Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 2,503 tubes are affected.
Product
Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate 3.5 mg, polymyxin B sulphate 5000 units, Net Wt. 0.5 oz (14g) tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2415-2026·2026-06-24
Medline nerve block trays contain recalled Mastisol liquid adhesive
Medline CCI Nerve Block Trays and CPNB kits are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2427-2026·2026-06-24
Medline hernia repair totes contain recalled Mastisol liquid adhesive
The Medline Hernia Repair Tote convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2434-2026·2026-06-24
Medline da Vinci main kits contain recalled Mastisol liquid adhesive
Medline da Vinci Main convenience kits are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kits: DAVINCI MAIN DYNJ908031D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0592-2026·2026-06-24
Kerr Insta-Char 50 gram charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char, 50 grams activated charcoal in a sorbitol base, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in 240 mL (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0632-2026·2026-06-24
Lil Drug Store triple antibiotic ointment recalled over manufacturing deviations
Lil Drug Store Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,225 tubes affected.
Product
Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g), Product distributed by: Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404, Made in India, UPC 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0588-2026·2026-06-24
Alyacen 7/7/7 birth control tablets failed total impurities specification
Alyacen 7/7/7 norethindrone and ethinyl estradiol tablets are being recalled because of out-of-specification results for total impurities.
Product
ALYACEN 1/35 — ALYACEN 1/35 (NORETHINDRONE AND ETHINYL ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0637-2026·2026-06-24
Med Pride bacitracin zinc ointment recalled over manufacturing practice deviations
Med Pride Bacitracin Zinc Ointment, 1 oz tubes, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,185 tubes affected.
Product
Med Pride, Bacitracin Zinc Ointment, 1oz (28.3g) per tube, 72 tubes per case, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC X004WB4LKT.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2429-2026·2026-06-24
Medline labor and delivery C-section kits contain recalled Mastisol adhesive
The Medline Labor & Delivery C-Section convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0636-2026·2026-06-24
Med Pride bacitracin zinc ointment 500 units recalled over manufacturing deviations
Med Pride Bacitracin Zinc Ointment, 500 units per gram in 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,374 tubes affected.
Product
Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30354 8.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0603-2026·2026-06-24
Burkhart benzocaine topical anesthetic gel bottles may have incomplete seals
Burkhart topical anesthetic gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units are affected.
Product
BURKHART TOPICAL ANESTHETIC — BURKHART TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2425-2026·2026-06-24
Medline IV start kits with HubGuard contain recalled Mastisol adhesive
The Medline IV Start Kit with HubGuard is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2026·2026-06-24
Lucky Super Soft athlete's foot cream recalled over manufacturing deviations
Lucky Super Soft Antifungal Athlete's Foot Cream, clotrimazole 1%, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,102 tubes affected.
Product
Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2442-2026·2026-06-24
Medline femoral block trays contain recalled Mastisol liquid adhesive
The Medline Femoral Block Tray is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B
Category
Medical Device
Distribution
Distributed nationwide