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 Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2019
EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Monarch Medical Technologies
FDA (openFDA device enforcement)
Reported Nov 20, 2019
ORTHOFIX Catalogue Number: ref 11007, drill bit diameter 4.8 MM LENGTH 280 MM, RX ONLY, Non Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix Srl
30 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Fire Roasted Medium Arriba! Bacon Salsa with Real Bacon NET WT 16 OZ. UPC Code: 033907 20513 1 packaged in a clear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Riba Foods Inc.
FDA (openFDA food enforcement)
Reported Nov 20, 2019
ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Nov 13, 2019
Giraffe OmniBed Carestation CS1 - Product Usage: The device can be operated as an incubator or as a warmer and can…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Golden Dragon Almond Cookies in 5 lbs. box, each 5 lbs. box contains 5, 100 count bags, UPC on box and inner bag: 0…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Dragon Fortune Cookies Co. Inc.
FDA (openFDA food enforcement)
Reported Nov 13, 2019
SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
StemPro¿ MSC SFM CTS"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex-Morrisville
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Season's Choice Raspberries (frozen): 12 ounce bags; Product of Chile. Item number: 076163-01 Aldi brand name Season's…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wawona Frozen Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2019
Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Whole Foods Market White Parkerhouse Rolls PLU 49557 NET WT. 0 lb 12 oz (340g) packaged in a clear plastic bag 12 rolls…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Nov 7, 2019
Rastelli Bros., Inc. Retira Productos De Carne De Res Debido A Una Posible Contaminacin Con Materia Extraa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rastelli
USDA FSIS
Reported Nov 6, 2019
A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For fracture fixation or reconstruction of the sternum.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alto Development Corp.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Inc.
FDA (openFDA drug enforcement)
Reported Nov 6, 2019
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Port full Access Tray Product Code: DT19330
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
HYTEC Stop Solution (Allergy), 300ml bottle containing 1N sodium hydroxide solution, Part # 308051, sold separately or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hycor Biomedical LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
C3 Wave App, v. 2.0.5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Illinois recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.