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.
5,830 stored notices name Illinois, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Illinois too — those are in the archive.
Reported Oct 21, 2026Updated Oct 26, 2026
NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product Code: N271H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jenavalve Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Magellan Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sarnova HC, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G L Mezzetta Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safeguard US Operating LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026
SIERRA NEVADA GRAZIERS RAW MONTEREY JACK NET WT. 8oz. (225g) ITEM 6400 Plant No. 06-325 Willows, California 95988 UPC:…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Sierra Nevada Cheese Company, Inc.
FDA (weekly enforcement report)
Reported Oct 7, 2026Updated Oct 13, 2026
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026
Apheresis Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American National Red Cross (The), Lewis and Clark Region
FDA (weekly enforcement report)
Reported Oct 7, 2026Updated Oct 13, 2026
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ASP Global, LLC.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Central California Blood Center
1 more product in this recall
FDA (weekly enforcement report)
Reported Oct 7, 2026Updated Oct 13, 2026
Coco G's Courmet Flaming Cheddar Hots, Spicy Cheddar Cheese Popcorn. Packaged in the following sized plastic bags: 1.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Coco G's Snack Foods, Inc.
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.