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 92619280 of 13,494 recalls

DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone 12 mg/ml/Baclofen 450 mcg/ml Recalled by Hartley Medical...

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
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 1 mg/ml Recalled by Hartley Medical Center Pharmacy,...

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
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Morphine Sulfate 1.5 mg/ml Recalled by Hartley Medical Center Pharmacy,...

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
DrugFebruary 2, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone Diacetate Injectable Suspension Recalled by Isomeric Pharmacy...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2016· Hospira Inc.

Recalled Item: Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

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

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 20 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Bonita Pharmaceuticals, LLC

Recalled Item: Menthocin Patch with Lidocaine-Strong (Menthol 5% Recalled by Bonita...

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
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 80 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 40 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 10 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Amerisource Health Services

Recalled Item: Candesartan Cilexetil Tablets Recalled by Amerisource Health Services Due to...

The Issue: Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: identified as a cloth fiber.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Presence of Particulate Matter: identified as cardboard.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Lack of Assurance of Sterility: potential for leaking containers which lacks...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in Recalled by...

The Issue: Presence of Particulate Matter: identified as dried skin.

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

Class I — Serious Health HazardOngoing
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