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. 2,750 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,750 in last 12 months

Showing 2290122920 of 55,304 recalls

FoodAugust 8, 2019· Keto Farms LLC

Recalled Item: Keto Farms Keto Snack Mix - Tomato Pepperjack Fruit & Recalled by Keto Farms...

The Issue: California Department of Public Health Inspection found that the allergen,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· Keto Farms LLC

Recalled Item: Keto Farms Keto Snack Mix - Raspberry Gouda Fruit & Recalled by Keto Farms...

The Issue: California Department of Public Health Inspection found that the allergen,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· FIRST START HOLDINGS INC

Recalled Item: Nosh Organic Fruit & Protein Soft Oat Bar Recalled by FIRST START HOLDINGS...

The Issue: Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· FIRST START HOLDINGS INC

Recalled Item: Nosh Organic Fruit & Protein Soft Oat Bar Recalled by FIRST START HOLDINGS...

The Issue: Fruit & Protein Soft Oat Bars have the potential to be contaminated with mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 8, 2019· Keto Farms LLC

Recalled Item: Keto Farms Keto Snack Mix - Strawberry Gouda Recalled by Keto Farms LLC Due...

The Issue: California Department of Public Health Inspection found that the allergen,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2019· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastronintestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...

The Issue: Complaints have been received concerning elevated rates of false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2019· Radiometer Medical ApS

Recalled Item: AQURE basic sytem Recalled by Radiometer Medical ApS Due to The firm has...

The Issue: The firm has become aware that there is a potential problem relating to the...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP Recalled by Glenmark...

The Issue: Temperature Abuse: Complaints received of liquidy texture.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Aesculap Implant Systems LLC

Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...

The Issue: possibility of the sterility batch being insufficiently sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Aesculap Implant Systems LLC

Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...

The Issue: possibility of the sterility batch being insufficiently sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Integra LifeSciences Corp.

Recalled Item: Integra Jarit GEMINI CLAMP 9 1/4 inch - used in Recalled by Integra...

The Issue: A small crack at the box lock corner may after multiple cleaning and...

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...

The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2019· Amys Kitchen Inc

Recalled Item: Amy's Bowls - Broccoli & Cheddar Bake Recalled by Amys Kitchen Inc Due to...

The Issue: Consumer complaints of black plastic found in product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2019· Preventice Services, LLC

Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...

The Issue: The device data being collected and transferred to the monitoring center may...

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

Class II — Potential Health HazardOngoing