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. 2,733 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,733 in last 12 months

Showing 2944129460 of 55,304 recalls

Medical DeviceJanuary 24, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...

The Issue: The recalling firm identified a software issue related to the Patient Line...

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

Class II — Potential Health HazardOngoing
DrugJanuary 24, 2018· JCB Laboratories LLC

Recalled Item: Cefuroxime Recalled by JCB Laboratories LLC Due to Subpotent Drug: The...

The Issue: Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 24, 2018· LivaNova USA Inc

Recalled Item: VNS Therapy Programming System Recalled by LivaNova USA Inc Due to...

The Issue: Unintended warning message displayed on generators programmed with a Model...

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

Class II — Potential Health HazardOngoing
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Reduced-Fat Plain Cream Cheese Recalled by Panera, LLC Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Reduced-Fat Wild Blueberry Cream Cheese Recalled by Panera, LLC Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Chive&Onion Reduced Fat Cream Cheese Spread Recalled by Panera, LLC...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Bell Plantation Inc.

Recalled Item: Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars Recalled...

The Issue: Analytical results for generic non-pathogenic E. coli surpassed firm's...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Plain Cream Cheese Recalled by Panera, LLC Due to Potential Listeria...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 24, 2018· Panera, LLC

Recalled Item: Panera Reduced-Fat Honey Walnut Cream Cheese Recalled by Panera, LLC Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2018· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...

The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2018· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...

The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2018· Biomerieux Inc

Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...

The Issue: Missing desiccant.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2018· Valeris Medical, LLC

Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...

The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...

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

Class II — Potential Health HazardOngoing
FoodJanuary 22, 2018· Sun Noodle New Jersey, LLC

Recalled Item: Sun Noodle brand Tonkotsu Ramen Recalled by Sun Noodle New Jersey, LLC Due...

The Issue: Product is labeled as Tonkotsu, but the actual flavor packet inside is...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 22, 2018· Mountain Rose Inc

Recalled Item: Prickly Ash Bark Powder Herbal Supplement Recalled by Mountain Rose Inc Due...

The Issue: Prickly Ash Bark Powder is recalled due to a potential contamination with...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 22, 2018· Ascent Pharmaceuticals, Inc.

Recalled Item: Oxycodone Hydrochloride Tablets Recalled by Ascent Pharmaceuticals, Inc. Due...

The Issue: Labeling; Label Error Not Elsewhere Classified; label missing controlled...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 22, 2018· Astellas Pharma US Inc

Recalled Item: Mycamine (micafungin) for Injection 100 mg/vial Single-Dose Vial Rx only...

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
Medical DeviceJanuary 21, 2018· SIE AG, Surgical Instrument Engineering

Recalled Item: The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8...

The Issue: This Correction is being initiated based on a customer complaint received on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2018· Mako Surgical Corporation

Recalled Item: Restoris MCK Onlay Insert Extractor. Recalled by Mako Surgical Corporation...

The Issue: Possible hinge pin disassociation from the Mako Onlay Insert Extractor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Flowmeter Module (accessory to Terumo Advanced Perfusion System 1). Provides...

The Issue: Inaccurrate flow readings. Depending on the degree of inaccuracy, this issue...

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

Class II — Potential Health HazardOngoing