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. 1,903 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,903 in last 12 months

Showing 4112141140 of 55,304 recalls

Medical DeviceJuly 7, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· Eizo Corporation

Recalled Item: RadiForce RX850 Recalled by Eizo Corporation Due to EIZO is recalling the...

The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· Eizo Corporation

Recalled Item: RadiForce RX650 Recalled by Eizo Corporation Due to EIZO is recalling the...

The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2015· Kremers Urban Pharmaceuticals, Inc.

Recalled Item: Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2) Recalled by Kremers...

The Issue: Failed Impurities/Degradation Specifications: Two lots failed specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2015· Kremers Urban Pharmaceuticals, Inc.

Recalled Item: Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2) Recalled by Kremers...

The Issue: Failed Impurities/Degradation Specifications: failed specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 6, 2015· BioComp Pharma, Inc.

Recalled Item: Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from:...

The Issue: Subpotent Drug: menthol and methyl salicylate below specification

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 6, 2015· Philips Electronics North America Corporation

Recalled Item: Actuator for angiographic x-ray monitor ceiling suspension system. Actuator...

The Issue: The actuator assembly became detached and the monitor carriage with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2015· CooperSurgical, Inc.

Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....

The Issue: Product marketed without a 510(k)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2015· Philips Electronics North America Corporation

Recalled Item: SENSE Body Coil 1.5T with identification Recalled by Philips Electronics...

The Issue: Wrong positioning of the coil cables can create unintended resonances via...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Potential...

The Issue: Potential issue leading to data loss and patient data mix-up

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

Class II — Potential Health HazardOngoing
FoodJuly 6, 2015· Mason Vitamins, Inc.

Recalled Item: Coenzyme Q-10 50 mg label reads in part Recalled by Mason Vitamins, Inc. Due...

The Issue: Product is mislabeled. Some of the Co Q 10 30 mg bottles were labeled with...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 3, 2015· NordicNeuroLab AS

Recalled Item: nordicICE v 2.3.14 nordicICE is an image processing software package...

The Issue: The bug causes BOLD activation maps to be visualized as overlays without...

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

Class II — Potential Health HazardOngoing
FoodJuly 2, 2015· Arthur Schuman Inc.

Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...

The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 2, 2015· Brett Anthony Foods

Recalled Item: Vegetable Chili Recalled by Brett Anthony Foods Due to Undeclared Milk

The Issue: The Vegetable Chili contains undeclared milk, an allergen.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2015· Stryker Medical Division of Stryker Corporation

Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...

The Issue: Customer complaints associated with faulty brake system

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2015· Stryker Medical Division of Stryker Corporation

Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...

The Issue: Inaccurate scale systems

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing