All recall categories

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.

Medical devices

Reported Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Diagnostics Scarborough, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abiomed, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2026

Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Acumed LLC

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

6/11oz Sunflower Seeds Salted

High riskUsing this product could cause serious injury, illness or death — stop using it now.

George J Howe Company, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ImpactLife

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2026

Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

Dried Herring Fish 7 oz.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Prime Food Processing LLC.

FDA (openFDA food enforcement)

Food

Reported Jul 1, 2026

Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Produce Innovations

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2026

INZONE DETACHMENT SYSTEM, REF: M00345100950

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Neurovascular

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Utz Quality Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Jun 25, 2026

FSIS Issues Public Health Alert for Boneless Chicken Breast Product Due to Misbranding and Undeclared Allergens

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

FW Farms LLC.

USDA FSIS

Medical devices

Reported Jun 24, 2026

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AMD Medicom Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Arrow International, LLC

34 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2026

azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Azuma Foods International Inc. USA

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

iLet Bionic Pancreas, REF: BB1001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Mito Red Light, Super Mobile

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mito Red Light Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2026

Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nutrisystem Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2026

Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Staar Surgical AG

FDA (openFDA device enforcement)

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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.