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.
Reported May 1, 2019
Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cytocell Ltd.
FDA (openFDA device enforcement)
Reported May 1, 2019
Edwards Lifesciences, Fogarty Dilation Atrioseptostomy Catheter, Sterile EO, Rx Only, REF: 830705F Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2019
Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
VITROS XT 7600 Integrated System, Product Code 6844461, UDI 1075870031658 Product Usage: The VITROS XT 7600 Integrated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported May 1, 2019
Thoratec HeartMate 3 Coring Tool, Sterile EO, Rx Only, REF 10005872, an optional accessory of Thoratec HeartMate 3 Left…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Apr 24, 2019
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device intended for use in bony voids or gaps that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bioventus, LLC
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cordis Corporation
FDA (openFDA device enforcement)
Reported Apr 24, 2019
NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton
High riskUsing this product could cause serious injury, illness or death — stop using it now.Little Red Rooster Company
FDA (openFDA food enforcement)
Reported Apr 24, 2019
Obturator (long cone), Part number 25162 Product Usage: The obturator is a component of the Flex Rectoscope which is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrobotics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed, Model 32/1. Labeled as the following: PROSUN ONYX 32 SLI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSun International, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2019
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Apr 17, 2019
Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Merical, LLC
FDA (openFDA food enforcement)
Reported Apr 17, 2019
Commercial Breader Batter; A28177 BATTER MIX X1; 50 pound bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Newly Weds Foods Inc.
30 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 17, 2019
AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Procept Biorobotics Corporation
FDA (openFDA device enforcement)
Reported Apr 17, 2019
syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2019
ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ulrich medical USA Inc.
FDA (openFDA device enforcement)
Reported Apr 10, 2019
The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2019
Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Century Snacks LLC
FDA (openFDA food enforcement)
Reported Apr 10, 2019
McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cypress Medical Products LLC
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.