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 Oct 21, 2020
Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Group Logistics America, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2020
SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handicare AB
FDA (openFDA device enforcement)
Reported Oct 21, 2020
TRADER JOE S TRADER POTATO TOTS is frozen potatoes, SKU # 94904, retail bag has net wt. 2 lbs. Product is packaged in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J .R. Simplot Company
FDA (openFDA food enforcement)
Reported Oct 21, 2020
Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Oct 14, 2020
MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2020
BellaTek Encode Defin3DPMSERitive Abutments-3D Printed Model Reference Numbers: 3DPMSER, 3DPMSERQ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2020
Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for Cranial/ENT Navigation 3.0.x and 3.1.x -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Oct 14, 2020
Diethylpropion, 25 mg tablets, Rx only, Distributed by: Calvin Scott & Co. Inc. Albuquerque, NM 87123; MFG. Lannett…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Calvin Scott & Company, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 14, 2020
DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instrument Tray for EMPOWR Porous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Oct 14, 2020
SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
FDA (openFDA food enforcement)
Reported Oct 14, 2020
Ground cinnamon. Packaged in bulk 50 lb. corrugated boxes with inside liner.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kalustyan Corp.
FDA (openFDA food enforcement)
Reported Oct 14, 2020
"Nettle Meadow Artisan Cheese *** Fig Honey Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz.***"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LuMaZu, LLC dba Nettle Meadow
4 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 14, 2020
Quick Release Gait Belt, 60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2020
DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2020
ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2020
PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a light cured, radiopaque, methacrylate based,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2020
Dual Mobility Vivacit-E Bearing, Model Number 110031009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2020
365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz. bag, UPC 099482428747, 16 retail units per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eagle Family Foods Group LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 7, 2020
Pacific Xtreme (PTCA Balloon Dilation Catheter)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ev3 Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2020
VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Speed Stitch Needle Cassette
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, modular, automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol, REF 33570.
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.