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. 2,915 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,915 in last 12 months

Showing 92819300 of 13,494 recalls

DrugJanuary 18, 2016· Amerisource Health Services

Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...

The Issue: Failed Dissolution Specifications: Unexplained low out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 15, 2016· Master Herbs, Inc./Li

Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...

The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 14, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: risperiDONE ORALLY DISINTEGRATING TABLETS Recalled by Zydus Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for a...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Real Skill Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Weekend Prince Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Hard Ten Days Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: African Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Herb Viagra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Plant Vigra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Man King Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull Recalled by R Thomas Marketing, LLC Due to Marketed Without An Approved...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Samurai-X Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Night Man Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund