Product Recalls in Illinois

Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,964 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,964 in last 12 months

Showing 4160 of 55,304 recalls

Medical DeviceFebruary 3, 2026· Exactech, Inc.

Recalled Item: Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit...

The Issue: Impactor handle may be missing cross-pin

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: It was identified that eh Universal Beam Triggering Interface (UBTI) is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Exactech, Inc.

Recalled Item: Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle...

The Issue: Impactor handle may be missing cross-pin

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 3, 2026· Pure Solutions, Inc.

Recalled Item: Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep...

The Issue: Label declares bovine colostrum but does not declare milk allergen.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION Recalled by B Braun...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Recalled by B...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2026· Pro Numb Tattoo Numbing Spray LLC

Recalled Item: Pro Numb Tattoo Numbing Spray Recalled by Pro Numb Tattoo Numbing Spray LLC...

The Issue: cGMP deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2026· Pro Numb Tattoo Numbing Spray LLC

Recalled Item: Pro Numb Tattoo Numbing Spray Recalled by Pro Numb Tattoo Numbing Spray LLC...

The Issue: cGMP deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INF SET Recalled by B Braun...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Covidien LLC

Recalled Item: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of:...

The Issue: Due to complaints and investigations stating that alarms from the primary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Medline Industries, LP

Recalled Item: Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit:...

The Issue: The instructions for use (IFUs) on specified Cardinal Health Chest Drainage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Beckman Coulter Mishima K.K.

Recalled Item: DxC 700 AU Recalled by Beckman Coulter Mishima K.K. Due to A delay in...

The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Beckman Coulter Mishima K.K.

Recalled Item: CHEMISTRY ANALYZER AU5800 Recalled by Beckman Coulter Mishima K.K. Due to A...

The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units...

The Issue: Potential for rubber fragment detachment during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2026· Teva Pharmaceuticals USA, Inc

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units...

The Issue: Potential for rubber fragment detachment during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 28, 2026· Art Monkey LLC dba Why Not Natural

Recalled Item: Why Not Natural Moringa Capsules 120 capsule bottle marked with Recalled by...

The Issue: Potential to be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund