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. 2,959 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,959 in last 12 months

Showing 13011320 of 55,304 recalls

DrugSeptember 25, 2025· SV Labs Prescott Corporation

Recalled Item: Aloe Up Sport Performance Sunscreen Lotion SPF 30 Recalled by SV Labs...

The Issue: cGMP deviations: the firm released and distributed product which failed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2025· DJO, LLC

Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...

The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· PHILIPS MEDICAL SYSTEMS

Recalled Item: Model: Incisive CT for Brazil SKD Recalled by PHILIPS MEDICAL SYSTEMS Due to...

The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· PHILIPS MEDICAL SYSTEMS

Recalled Item: Model: CT 5300 Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...

The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· BALT USA, LLC

Recalled Item: Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Recalled...

The Issue: Due to an identified manufacturing defect involving coating material lifting...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 25, 2025· PHILIPS MEDICAL SYSTEMS

Recalled Item: Model: Incisive CT Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...

The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...

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

Class II — Potential Health HazardOngoing
FoodSeptember 24, 2025· Now Foods

Recalled Item: NOW Real Food Organic Unsalted Whole Raw Cashews Recalled by Now Foods Due...

The Issue: Undeclared pine nut

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...

The Issue: Failed impurity/degradation specifications:Out of Specification result for...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...

The Issue: Failed impurity/degradation specifications:Out of Specification result for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2025· Stryker Sustainability Solutions

Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...

The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
FoodSeptember 23, 2025· Optiwize Inc.

Recalled Item: OptiWize Health OptiWize Collagen Plus 320 count bottle Recalled by Optiwize...

The Issue: The firm initiated a voluntary recall after NSF testing showed that labeled...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2025· ACME UNITED CORPORATION

Recalled Item: Sting Relief Swabs Recalled by ACME UNITED CORPORATION Due to Product Mix-up

The Issue: Product Mix-up

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2025· Total Joint Orthopedics, Inc.

Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...

The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2025· Becton Dickinson & Co.

Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...

The Issue: Product service credentials used by some BD technical support teams to...

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

Class II — Potential Health HazardOngoing