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

Food

Reported Apr 1, 2015

HEB Bean & Cheese Dip 9 oz. UPC: 041220804016

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

Dursett Amigos, Ltd.

10 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

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)

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)

Medical devices

Reported Mar 25, 2015

Medtronic, 10 Fr FlexCath Select Steerable Sheath 990065. The FlexCath Select Steerable Sheath (10 Fr Select) is used…

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

Medtronic Inc. Cardiac Rhythm Disease Management

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.

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

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…

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

GE Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY,…

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

Microport Orthopedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in…

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

Pivotal Health Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

Juno DFR X-ray system

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

Villa Radiology Systems LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2015

DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2

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

iCAD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: The titanium alloy set screw is used to seat a 5.5 mm titanium…

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

Biomet Spine, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…

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

GE Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…

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

Invacare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

Philips Multi Diagnost Eleva II

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

Philips Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…

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

Zimmer GmbH

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2015

Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2015

MC-500 Multicolor Laser Photocoagulator; Indicated for use in retinal photocoagulation for treatment of ocular fundus…

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

Nidek Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2015

Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly…

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 20, 2015

ESS Food Recalls Pork Products Produced Without Benefit of Import Inspection

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

ESS Food

USDA FSIS

Medical devices

Reported Feb 18, 2015

The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…

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

Integra LifeSciences Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2015

MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…

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

Kellogg USA Inc.

1 more product in this recall

FDA (openFDA food 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.