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. 2,909 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,909 in last 12 months

Showing 1054110560 of 13,494 recalls

DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP Recalled by...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP 25 Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 12, 2015· Stroheckers Inc Pharmacy

Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil Recalled by Stroheckers Inc...

The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 10, 2015· Medtech Products, Inc.

Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule...

The Issue: Marketed without an approved NDA/ANDA: The distributed units of Monistat 1...

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Akorn, Inc.

Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Sterility Assurance: The product has the potential to leak at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Akorn, Inc.

Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 2, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: Acarbose Tablets 50 mg a)10 x 10 Unit Dose Tablets per Blister Pack Recalled...

The Issue: Subpotent Drug: The firm received an out of specification result for Assay...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2015· Cody Laboratories, Inc.

Recalled Item: C-Topical 4% CII (cocaine hydrochloride) Recalled by Cody Laboratories, Inc....

The Issue: Labeling: Label mix-up; bottles were incorrectly labeled as 10 mL instead of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Cartia XT (diltiazem HCl extended-release capsules Recalled by Actavis...

The Issue: Presence of Foreign Substance; fine residue or dust identified as aluminum...

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

Class III — Low RiskOngoing
Refund
DrugMarch 26, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: the manufacturer, recalled...

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

Class III — Low RiskOngoing
Refund