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 48,132 notices were distributed nationwide, so they reach Illinois too — those are in the archive.

Medical devices

Reported Apr 8, 2015

Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a…

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

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2015

Mrs. Fields White Chunk Macadamia Cookies; 12 individually wrapped cookies in a tray/box; there are 6 trays/boxes to a…

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

Interbake Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Double Swivel Connector with Suction Port Connector, Airway (Extension) King Systems part 7169 Product Usage: An airway…

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

King Systems Corp.

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 8, 2015

La Guadalupana Wholesale Co. Retira Productos Carne De Res Y Pollo Debido A Que Fueron Producidos Sin El Beneficio De…

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

La Guadalupana

USDA FSIS

Medical devices

Reported Apr 8, 2015

Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…

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

Medtronic Inc. Cardiac Rhythm Disease Management

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

Hellas Golden Double Smoked Herring Vacuum Karagounis Bros SA -Hellas -35 A.3 - C.E. 2nd Industrial Zone -37500 VOLOS…

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

Moscahlades Bros Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when…

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

Orthovita, Inc., dba Stryker Orthobiologics.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by…

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

Owen Mumford USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.

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

Quest Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part…

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

Synthes, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2015

Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75")…

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

Ameda, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2015

BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2015

8 in. sundried tomato flavored tortilla wraps, packaged in re-sealable polypropylene bags, 10 wraps per bag. Sold under…

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

El Popocatepetl Ind., Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 1, 2015

Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…

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

fgf brands, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2015

Variable Angle Locking Peg, D:1.8mm x L:14.0mm; Variable Angle Locking Peg, D:1.8mm x L:16.0mm, Variable Angle Locking…

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

Flower Orthopedics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2015

Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform immunohistochemical (IHC) staining. Product…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2015

Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067.…

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

Philips Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2015

Stonewall Kitchen Buffalo Wing Sauce Net Wt. 17.5 oz. glass jar UPC 711381-31395 4 Item # 251805,

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Food

Reported Apr 1, 2015

Frozen vegetable-based burgers RETAIL - DOMESTIC: Organic Sunshine Burgers Gluten Free Soy Free Vegan Barbecue 3…

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

Sunshine Burger & Specialty Food Company, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2015

Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is…

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

Titan Spine, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2015

Wal-Mart private label "the Bakery baked with pride," Sock It To Me Cr¿me Cake, Net Wt. 32oz (2lb) 907g, (packed in a…

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

Benson's Old Home Kitchens Bakery Division

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2015

Crea A and B membranes, packaged 4 per box Used in conjunction with the ABL800 FLEX analyzers which are intended for:…

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

Radiometer America 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.