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 Apr 13, 2022

SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x

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

Volcano Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b)…

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

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.

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

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Hanger-Bar 2P 45cm

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

Human Care USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Illumina NextSeq 550Dx, REF: 20005715, CE, IVD

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

Illumina, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…

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

Medtronic MiniMed

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Pneumonia (33 Targets) Control Panel, unassayed quality control material, containing: Positive Control 1 -…

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5…

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

RaySearch America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

TomoHelical and TomoDirect plans in RayStation 6, 7, 8A, 8B, 9A, 9B, 10A, 10B and 11A. Build Numbers: 6.1.1.2, 6.2.0.7,…

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

Raysearch Laboratories Ab

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

cobas LiatSystem, respiratory virus panel nucleic acid assay system, Material Number 07341920190

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

Roche Molecular Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 6, 2022

Good & Gather Dried Sweetened Strawberries. Net Wt 4 oz (113g). UPC 085239-182840 No Sulfites Added. No Artificial…

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

Suntree Snack Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 30, 2022

BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373,…

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

Biomet, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 30, 2022

Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml 12 units per case . Tetra Pak paper carton.

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

Flow Beverages Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 30, 2022

Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 30, 2022

Shredded Cheese consisting of Monterey Jack, Queso Quesadilla, and Asadero cheeses, Net Wt 2lbs, packaged in plastic…

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

Schreiber Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 23, 2022

Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended…

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

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer

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

Bard Peripheral Vascular Inc.

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 23, 2022

Rosarita Organic Refried Beans Multipack carton containing 8 - 16oz cans

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

ConAgra Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 23, 2022

Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container.…

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

Fdmr, Inc. dba Suji's Korean Cuisine

FDA (openFDA food enforcement)

Medical devices

Reported Mar 23, 2022

(1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX…

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

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X…

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

Hologic, Inc.

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.