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 48,100 notices were distributed nationwide, so they reach Illinois too — those are in the archive.
Reported Feb 8, 2023
CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smiths Medical ASD Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2023
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Veritas Advanced Infusion Packs, REF: VRT-AI
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2023
CENTURION MEDICAL PRODUCTS, SILVER ANTIMICROBIAL VAD DRIVE, REF DT18760
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Feb 1, 2023
FentaNYL Citrate 2.5mg/50mL (50mcg/mL) Injection Solution, Preservative-Free IV Injection 50mL Cassette, Rx Only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OurPharma LLC
FDA (openFDA drug enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2023
Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jan 25, 2023
Rasagiline Mesylate Tablets 1 mg; 30 tablets in HDPE bottle; Rx only; NDC 67877-260-30; Manufactured by Alkem…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Jan 25, 2023
Greco and Sons Dough Room Product No. 333 PUB DOUGH 9 oz.; Greco and Sons Dough Room Product No. 88 Christopher's 14…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sysco Merchandising and Supply
8 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 25, 2023
Pasta Para Duris 12 oz. (340g) Brand Name: Melissa's UPC: 045255 152739 Distributed by: World Variety Produce, Inc. PO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Variety Produce Inc. dba Melissa's
FDA (openFDA food enforcement)
Reported Jan 18, 2023
BD Pyxis MedBank System - Product Label/labeling pending
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
DeRoyal ORGAN RECOVERY PACK PGYBK, a) REF 89-9004.09 and b) 89-9004.10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Medical Industries, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Medline CISION Sterile Blades. Labeled as follows with corresponding Item Number. a. STERILE BLADE NO. 10 CARBON STEEL,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Jan 18, 2023
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
True Goodness by Meijer Oat-Based Plain Yogurt Alternative, 24oz plastic tub, UPC: 7-13733-03918-5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meijer Inc.
FDA (openFDA food enforcement)
Reported Jan 18, 2023
Beijing Hawthorne Candy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Jan 18, 2023
Stradis Healthcare Foley Catheter Insertion Tray with preconnected bag and catheter, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
Members Mark Holiday Macarons 540g units in plastic trays, 10 units per case Keep frozen, refrigerate after opening…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sublime Desserts Inc.
FDA (openFDA food enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2023
"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Jan 4, 2023
Pilling Wecksorb Cylindrical Sponges
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Premium Quality Shirakiku Fish Sausage Original Net wt. 9.8 oz. (280g) UPC 074410366414 Ingredients: Fish meat (bream,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wismettac Asian Foods, Inc.
1 more product in this recall
FDA (openFDA food 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.