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. 2,730 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,730 in last 12 months

Showing 3200132020 of 55,304 recalls

DrugMay 30, 2017· Mckesson Packaging Services

Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 26, 2017· Smucker Foods of Canada Co.

Recalled Item: Golden Temple No. 1 Fine Durum Atta Flour Blend NET Recalled by Smucker...

The Issue: The firm was notified by their Co-packer that the product may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Smucker Foods of Canada Co.

Recalled Item: Flour sold under the following brands: Golden Temple Durum Atta Flour Blend...

The Issue: The firm was notified by their Co-packer that the product may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET...

The Issue: The firm was notified that the product may contain peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE Recalled...

The Issue: The firm was notified that the product may contain peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 25, 2017· AstraZeneca Pharmaceuticals, LP

Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...

The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 25, 2017· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...

The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...

The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Atrium Medical Corporation

Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...

The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer Recalled by Exactech,...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: Logic Fit Tibial Tamp Head Recalled by Exactech, Inc. Due to The firm...

The Issue: The firm determined that the labeling (surgical technique) should be updated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Carestream Health Inc

Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...

The Issue: Carestream found a single unit where four screws in the assembly were not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...

The Issue: Presence of foreign substance: The recall was initiated due to black...

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

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund