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 Sep 26, 2018

Temperature sensor Foley catheter 18FR, Catalogue Number 102205101880AB Product Usage: This is sterile, single use,…

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

Degania Silicone, Ltd.

31 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

PR1000 Pivot Rehab Bed AC powered adjustable bed.

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

Med-Mizer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

Endoscopic Cleaning Brush, single use, sold in kits and labeled as the following: a. Item Number DYK1002DCB, BRUSH,…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 26, 2018

White Corn Tortilla Chips packaged under the following brand names and sizes: 1. Shearer's White Restaurant Style Bulk,…

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

Shearers Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 19, 2018

Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model Number 8445000 Product Usage: The…

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

Beaver Visitec

FDA (openFDA device enforcement)

Medical devices

Reported Sep 19, 2018

CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 19, 2018

da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 19, 2018

Tyvaso Inhalation System Patient a) Starter Kit with TYVASO (treprostinil) Inhalation Solution. Treprostinil 1.74…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

United Therapeutics Corp.

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 19, 2018

Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280

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

Zimmer Biomet, Inc.

128 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Alden Optical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD)

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 12, 2018

Fresh Express Chopped Romaine 1 lb

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

Fresh Express Incorpated

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 12, 2018

VidiStar(TM) PACS & DICOM Viewer Software system

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

Hitachi Healthcare Americas Corp. Informatics Division

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep Apnea, Inspire Part #900-003-020, Product…

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

Inspire Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

Baby Quasar Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.

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

Quasar Bio-Tech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 12, 2018

Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Virtus Pharmaceuticals Llc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 12, 2018

Outer Package Label: Tapered Screw-Vent Implant System, 4.1mm X 10mm, 3.5mm, REF:TSVM4B10, Sterile:R, Rx Only; Inner…

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

Zimmer Dental Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 5, 2018

Caito Foods, LLC Retira Productos De Ensalada De Pollo Debido A Un Error De Rotulacin Y Un Alrgeno No Declarado

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

Caito Foods, LLC

USDA FSIS

Food

Reported Sep 5, 2018

Premo Brand Turkey & Cheese Wedge sandwiches 5 OZ retail UPC 612510002018 Plastic triangle sandwich wedge container…

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

Lipari Foods Operating Company, LLC dba JLM Manufacturing

FDA (openFDA food enforcement)

Medical devices

Reported Sep 5, 2018

Verigene Enteric Pathogens Nucleic Acid Test (EP) for detecting and identification of pathogenic enteric bacteria,…

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

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Other states

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.