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. 1,137 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,137 in last 12 months

Showing 16061–16080 of 55,304 recalls

Medical DeviceAugust 13, 2021· Quidel Corporation

Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...

The Issue: Revised Instructions for Use: Potential for specimens from patients with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· IMPERATIVE CARE INC

Recalled Item: Imperative Care Recalled by IMPERATIVE CARE INC Due to There is a potential...

The Issue: There is a potential for distal end of catheters to fracture and become...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring Recalled by Greiner...

The Issue: Blood collection tubes may experience a clotting issue.

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

Class II — Potential Health HazardOngoing
FoodAugust 13, 2021· Hostess Brands, LLC

Recalled Item: Hostess Soft White Hot Dog Buns Recalled by Hostess Brands, LLC Due to...

The Issue: The firm's contract manufacturer found positive environmental samples...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 13, 2021· Hostess Brands, LLC

Recalled Item: Hostess Soft White Hamburger Buns Recalled by Hostess Brands, LLC Due to...

The Issue: The firm's contract manufacturer found positive environmental samples...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate POWDER Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Failed Impurities Specifications: Out of Specification impurity results...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Zydus Pharmaceuticals (USA) Inc

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

The Issue: Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Akorn, Inc.

Recalled Item: Betamethasone Dipropionate Lotion USP (Augmented) Recalled by Akorn, Inc....

The Issue: Failed impurities/degradation specification: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg/1mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2021· AMTEC SALES Inc

Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 7.0 Recalled by GE Healthcare, LLC Due to A...

The Issue: A software anomaly exists in the Centricity Universal Viewer study...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: LikoStretch 1900 Model Number: 3156051 - The combination of this Recalled by...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing