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 48,122 notices were distributed nationwide, so they reach Illinois too — those are in the archive.

Medical devices

Reported Nov 6, 2019

Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…

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

OrthoPediatrics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…

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

Pajunk GmbH

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…

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

Rong Shing Trading NY Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Posey Connected Twice-As-Tough Cuffs

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

Tidi Products

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

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

Andover Healthcare Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm

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

CrossRoads Extremity Systems, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

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

IrriMAX Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz., with UPC code 612510002032.

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

Lipari Foods Operating Company, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic…

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

Mrs. Stratton's Salads, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral component of a primary…

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

OMNIlife science Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…

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

Roland Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for:…

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

Threshold Enterprises Ltd.

FDA (openFDA food enforcement)

Food

Reported Oct 30, 2019

Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base, 435G SK, UPC 074410455200 Distributed by…

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

Wismettac Asian Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 23, 2019

Orchids Dried Mushroom NET WT. 1 oz. (29G) Product of China UPC 0-74601-00947-2 Distributed by CTC Food International,…

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

CTC Food International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 23, 2019

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…

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

ICU Medical Inc.

21 more products in this recall

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.