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. 1,028 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,028 in last 12 months

Showing 39161–39180 of 55,304 recalls

DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Oasis Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: Asset BOLD Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SlimeX-15 Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...

The Issue: On a rare occasion, there is a potential to assign a patient result to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...

The Issue: The door latch may not fully close and the door may open unexpectedly. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...

The Issue: An issue with the Panorama Central Station may cause the system to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

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

Class III — Low RiskOngoing
FoodDecember 14, 2015· Sun Noodle New Jersey, LLC

Recalled Item: Tonkutsu Ramen Recalled by Sun Noodle New Jersey, LLC Due to Undeclared Eggs

The Issue: Tonkutsu Ramen may contain undeclared eggs.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 11, 2015· Sweet Superior Ltd

Recalled Item: PICOSITO Jalapenos Distributed by: Sweet Superior Fruit LTD. CO. PRODUCE...

The Issue: Tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 11, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...

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

Class III — Low RiskOngoing
DrugDecember 11, 2015· Reesna, Inc

Recalled Item: FUEL UP PLUS Recalled by Reesna, Inc Due to Undeclared Hydroxythiohomosildenafil

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 11, 2015· Reesna, Inc

Recalled Item: FUEL UP HIGH OCTANE Recalled by Reesna, Inc Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 10, 2015· Pine Valley Foods Inc

Recalled Item: Crazy about Cookies 2lb Birthday Celebration COLLECTION Decorated SUGAR...

The Issue: Pre-portioned sugar cookie dough contains undeclared milk and pre-portioned...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 10, 2015· Pine Valley Foods Inc

Recalled Item: Crazy about Cookies 2lb Monster Bash COLLECTION Decorated SUGAR COOKIE...

The Issue: Pre-portioned sugar cookie dough contains undeclared milk and pre-portioned...

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

Class I — Serious Health HazardOngoing
Refund