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 Apr 8, 2020
Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Guan's Enoki Mushrooms; Net Weight 200 g - 7.05 oz. UPC: 8 59267007013 Product Number:50130 Product of Korea, Keep…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Forest Mushroom Food Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care of a healthcare professional, Gentell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gentell, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Meijer Mixed Nuts with Peanuts & Sea Salt 16 Oz UPC: 7-19283-80863-9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meijer Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Nature's Blend Folic Acid 1000 mcg Dietary Supplement, 1000-count bottle, Product Number: 1280, UPC 0-79854-51280-9
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.National Vitamin Company Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2020
Philips V60 Ventilators with Power Management PCBA part number 1055906
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
FDA (openFDA device enforcement)
Reported Apr 8, 2020
NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusable instrument designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2020
Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical, LLC
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diabetes Care, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
LN 3R70-01; software version 2.6.2 and earlier. The software is used with the Alinity i (LN 03R65-01) processing module…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Apr 1, 2020
American Classic Snack Company Sweet Bourbon Crunchers Pretzels in 8 oz. bags, 12 bags per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Classic Snack Co., LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Aseltines 100% JUICE Apple Cider 1/2 gallon UPC 5169600064 and 1 gallon UPC 5169600128
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aseltines
FDA (openFDA food enforcement)
Reported Apr 1, 2020
1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Baskin Robbins Mint Chocolate Chip, Ice Cream Sandwiches with Mint Ice Cream, Semi-Sweet Chocolate Chips & Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dean Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Enoki Mushroom; Product of Korea; Net Wt. 7.05 oz., (200 g) UPC: 7 426852 625810 The Enoki is packaged in a clear film,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hong Bin Foods LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Clover seed in 50 lb. woven poly bags, 40 bags to a pallet.
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holding Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Cardiovascular Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
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.