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 78417860 of 13,494 recalls

DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: G.A.C 25/100/250mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Calcium chloride 10% Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 11, 2017· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Phentermine Capsules Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...

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

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

Class III — Low RiskOngoing
Refund
DrugAugust 10, 2017· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Amoxicillin and Clavulanate Potassium for Oral Suspension Recalled by Morton...

The Issue: Presence of Foreign Substance: customer complaint of blue foreign material...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2017· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2017· Degasa Sa De Cv

Recalled Item: Povidone Iodine Recalled by Degasa Sa De Cv Due to Labeling: Label mix-up....

The Issue: Labeling: Label mix-up. Finished product Povidone iodine 7.5% was labeled as...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugAugust 3, 2017· MEDLINE INDUSTRIES INC

Recalled Item: Vitamin A&D Ointment (petroleum 93.5%) Recalled by MEDLINE INDUSTRIES INC...

The Issue: Labeling Mixup; the individual A&D ointment foil packets are incorrectly...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2017· KVK-Tech, Inc.

Recalled Item: Phentermine HCL Capsules Recalled by KVK-Tech, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugAugust 3, 2017· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Lorazepam Oral Concentrate Recalled by Amneal Pharmaceuticals of New York,...

The Issue: Defective Delivery System: the dropper measurement markings may be reversed,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Diocto Liquid Recalled by The Harvard Drug Group Due to Microbial...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Diocto Syrup Recalled by The Harvard Drug Group Due to Microbial...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Glipizide Extended-Release Tablets (anti-diabetic agent) Recalled by Teva...

The Issue: Failed Moisture Limits: out of specification test results for water content...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Senexon Liquid Natural Vegetable Stimulant Recalled by The Harvard...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Major Senna Syrup Natural Vegetable Laxative Recalled by The Harvard Drug...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Aller-chlor (Chlorpheniramine Maleate Syrup Recalled by The Harvard...

The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2017· The Ampt Life, LLC

Recalled Item: NATURAL HERBAL COFFEE AMPT Recalled by The Ampt Life, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 28, 2017· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specification: out of specification for tablet weight.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund