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

Medical devices

Reported Jul 16, 2014

Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

BD FACS Canto and associated Fluidics Cart Product Usage: Flow cytometer for use in In vitro Diagnostics.

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

BD Biosciences, Systems & Reagents

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…

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

Global Cooling Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

Laceration Trays, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc., Arden, NC.

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

Medical Action Industries Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2014

Ocean Spray¿ Greek Yogurt Covered Craisins¿ Dried Cranberries , 8 oz Resealable Pouch UPC: #23719

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

Ocean Spray Cranberries Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2014

BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2014

Physique Enhancing Science ALPHAMINE, Powerful Thermogenic Powder, DIETARY SUPPLEMENT Net Wt. 8.9 oz (252 g). Raspberry…

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

Physique Enhancing Science

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 2, 2014

Dark Old Fashioned Sponge Candy, sold under the following brand and sizes: 1. Eillien's in Net Wt. 6 oz (170g) UPC…

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

Eillien's Candies, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2014

MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

ANSPACH***Knotless Suture Anchor Deployment Tool, Custom***Rx Only*** This device is intended to be used with Anspach…

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

The Anspach Effort, Inc.

44 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 25, 2014

liveGfree Gluten Free Blueberry Pancakes NET WT 14.4 OZ, 12 pancakes Keep Frozen Distributed By Aldi, Inc., Batavia, IL…

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

American Waffle

FDA (openFDA food enforcement)

Food

Reported Jun 25, 2014

Fayette Creamery Jalapeno Pepper Raw Milk Cheddar Cold Pack Cheese, Net Wt. 8 oz (226g), UPC 09513-00008

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

Brunkow Cheese

FDA (openFDA food enforcement)

Medical devices

Reported Jun 25, 2014

Synergy XVI Intended for radiation therapy treatment.

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

Elekta, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 25, 2014

Iowa Firm Recalls Sausage Products Containing Soy and Wheat Due to Misbranding and Undeclared Allergens

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

K & W Sausage

USDA FSIS

Medical devices

Reported Jun 25, 2014

Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

VersaCell X3 Solution and VersaCell X3 Expansion Pack, a robotic laboratory sample-management system. It connects up to…

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

Siemens Medical Solutions Diagnostics

FDA (openFDA device enforcement)

Food

Reported Jun 18, 2014

Poco Pac Salad Dressing, Distributed by Diamond Crystal Brands, Inc., Savannah, GA 31405, and packaged in single serve…

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

Diamond Crystal Brands, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2014

Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management application that is…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive (BioGlue) is indicated for use as an adjunct to…

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

CryoLife, Inc.

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.