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. 2,943 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,943 in last 12 months

Showing 43014320 of 13,494 recalls

DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 16, 2020· Perrigo Company PLC

Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2020· Calvin Scott & Company, Inc.

Recalled Item: Diethylpropion Recalled by Calvin Scott & Company, Inc. Due to cMGP...

The Issue: cMGP Deviations: Drug products repackaged into pouches without supporting...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phentermine Recalled by Calvin Scott & Company, Inc. Due to cMGP Deviations:...

The Issue: cMGP Deviations: Drug products repackaged into pouches without supporting...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2020· Calvin Scott & Company, Inc.

Recalled Item: Diethylpropion Recalled by Calvin Scott & Company, Inc. Due to cMGP...

The Issue: cMGP Deviations: Drug products repackaged into pouches without supporting...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2020· Arbor Pharmaceuticals Inc.

Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Panagel Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2020· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical...

The Issue: Failed Impurities/Degradation Specifications; high out of specification...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 4, 2020· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine Transdermal System 5 mcg/hour Recalled by Teva Pharmaceuticals...

The Issue: Failed Stability Specifications: Below specification result for...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2020· Akorn, Inc.

Recalled Item: Eye Itch Relief Recalled by Akorn, Inc. Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 2, 2020· pH-D Feminine Health

Recalled Item: pH-D Feminine Health Boric Acid Vaginal Suppositories Recalled by pH-D...

The Issue: Marketed without an Approved NDA/ANDA.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2020· The Protein Shoppe

Recalled Item: Red-E Tablet Recalled by The Protein Shoppe Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA: product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund