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 Mar 6, 2024
In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit, REF 01N15-010; (2) Abbott Vysis LSI D13S319…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Molecular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EMD Millipore Corporation
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Neurosurgery
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2024
MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mutti USA Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2024
NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NxStage MDS Corporation
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Oggi Pizza Plant Based Americana Beyond Meat Crumbles on Cauliflower Crust, gluten-free frozen pizza - cook before…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pasta Oggi Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2024
Cotija cheese packaged in the following configurations: 1. Sargento Course Grated Cotija Cheese Pack Size 6/5 lb.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sargento Foods, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2024
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
FDA (openFDA device enforcement)
Reported Feb 28, 2024
Voriconazole for Oral Suspension, 40mg/mL, Orange-Flavored, 49g/75mL when reconstituted. Mixing Directions: Tap the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Feb 28, 2024
Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Procter & Gamble Company
FDA (openFDA food enforcement)
Reported Feb 28, 2024
Aligned Medical Solutions, Local Lower Extremity Pack I, AMS10833, STERILEEO
High riskUsing this product could cause serious injury, illness or death — stop using it now.Windstone Medical Packaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Gluten Free Bean and Cheese Burrito (5.5 oz), individual plastic overwrap, 12 retail units/case, frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amy's Kitchen Inc.
FDA (openFDA food enforcement)
Reported Feb 21, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM 350P/350-UNIT-US-10, 350-STR-US-10,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuroLogica Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2024
CombiDiagnost R90 1.0 (709030)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.S. Tov, Inc.
FDA (openFDA food enforcement)
Reported Feb 21, 2024
3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
1 more product in this recall
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.