All recall categories

Recalls distributed in Iowa

These notices name Iowa 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.

2,845 stored notices name Iowa, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Iowa too — those are in the archive.

Food

Reported Dec 26, 2018

Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per case UPC #: 863669742526 refrigerate after opening

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

Lipari Foods Operating Company, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 19, 2018

Apricot Chai Tea, 8 oz. Loose. UPC 41427-96317

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

Cedar Lake Tea

FDA (openFDA food enforcement)

Food

Reported Dec 19, 2018

Imperial Taste Fried Red Onion, Cu Hanh Phi; 24 x 8oz. Item #1760, UPC Code: 741861017607; 24 x 12oz. Item #1761, UPC…

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

Gemini Food Corporation Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2018

Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare…

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

Heartware, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050…

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

Neotract Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 19, 2018

Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1 ounce and 16.5 ounce cardboard boxes. Distributed by The…

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

Quaker Manufacturing, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2018

Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in, 10 CT. White, bleached, non-woven, rayon/polyester sterile…

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

Aso, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2018

Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077

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

Capintec Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2018

16 count Smartfood Delight Variety Pack Sack

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

Frito-Lay, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2018

Smartypants Kids Complete, Non GMO Multi and omega 3's vitamin D3 for bones, vitamin B12 for Energy: 90 gummies. UPC 8…

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

Smartypants Vitamins

FDA (openFDA food enforcement)

Food

Reported Dec 5, 2018

Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261…

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

Chukar Cherry Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 5, 2018

QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part…

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

Maquet Cardiovascular US Sales, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2018

Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars12x100mm - Product Usage:…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Irrisept OR, Finished Bottle Assembly 450 ml STEP 1

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…

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

Merck Millipore Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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

Stryker Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2018

Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs

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

The Wornick Company

FDA (openFDA food enforcement)

Medical devices

Reported Nov 14, 2018

FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product…

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

Integrity Implants Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform…

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

Qiagen Sciences LLC

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.