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 Aug 8, 2018

Nicolet¿ Ambulatory EEG

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

Natus Neurology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Zimmer Dermatone AN, Model No. 88710100

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the…

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

Ad-Tech Medical Instrument Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg…

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

Ampi

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…

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

Bio-Rad Laboratories Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2…

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

Biscomerica, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

Access Hi-Low Exam Tables, Model 6501-XX

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

Brewer Company, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Brivo XR385, model 5215463, Digital Diagnostic Radiographic System

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…

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

GE Medical Systems, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model…

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

Medela Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Nobel Biocare 17¿ Multi-Unit Abutment, Conical Connection NP, 2.5mm, REF 36614. Product Usage: Intended to be used in…

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

Nobel Biocare USA LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

OMNI Hip System, ApeX-LNK Acetabular Inserts 0 degree, 4+mm offset, Product Codes: H6-14436, H6-13928 & H6-14836…

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

OMNIlife science Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

Amino Life brand Product - L-Leucine Instant Sunflower 25 Kgs Fiber carton double layer polyethylene bag as liner

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

Prinova US LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

ARTIS Pheno, Fluoroscopic X-Ray system, Model Number 10849000

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

BLAST Bandage, sterile.

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

Tactical Medical Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031

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

Ethicon, Inc.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended…

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

GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part Number 9735559, Visualase¿ Cooled Laser Applicator…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012…

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

Opgen Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),…

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

Raysearch Laboratories Ab

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.