All recall categories

Recalls distributed in Illinois

These notices name Illinois in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

5,761 stored notices name Illinois, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Illinois too — those are in the archive.

Medical devices

Reported Feb 17, 2021

Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arjohuntleigh Magog, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cytocell Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

60 IN (152cm) APPX 1.5 ml, PUR YELLOW SMALLBORE SET, FILTER REF B2209 - Product Usage: The intravascular administration…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

WAHL 4212 HEATED MASSAGER, SKU F800000004212 - Product Usage: intended to relieve minor muscle aches and pains.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wahl Clipper Corp.

FDA (openFDA device enforcement)

Food

Reported Feb 17, 2021

Reese Bearnaise Sauce packaged in glass jars 7.5 oz UPC: 7067060109

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

World Finer Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 10, 2021

Amy's Soups made with organic Lentils - Golden Lentil - Indian Dal. Net Wt. 14.4 oz (408g) Ready to serve - do not add…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2021

FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2021

Neuroreader Medical Image Processing Software - Product Usage: intended to automate the current manual process of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brainreader ApS

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2021

Dole Endless Summer Salad Kit; 13 oz. bag UPC: 0-71430-01073-0 Contains Milk, Wheat Distributed by Dole Fresh…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2021

Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2021

Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2021

SARS-CoV-2 Antigen Test

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 5, 2021

Food Evolution Recalls Ready-to-Eat Dip and Salad Products Containing Meat Produced Without Benefit of Inspection

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Food Evolution

USDA FSIS

Medical devices

Reported Feb 3, 2021

BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Braxton Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 3, 2021

Blueberry Blizzard Coffee Cake, Item 259, Net Wt. 24 oz.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nueske Applewood Smoked Meat, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 3, 2021

AK 10 5/8" Par Baked Stuffed Crust, frozen Pizza Crust, Item 1115660, Case Count / Unit Weight, 283 Count / 21.5 oz.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Port City Bakery, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 3, 2021

Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Respironics California, LLC

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 2, 2021

FSIS Issues Public Health Alert for Raw Ground Beef Product Due to Possible E. Coli O157:H7 Contamination

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Medical devices

Reported Jan 27, 2021

ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.