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.
Reported Dec 19, 2012
WANG Transbronchial Aspiration Needles Cat. No. MW-222, WANG Cytology Needles, Central or Peripheral Regions, 22 g x 13…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
DPM 6/7 Patient Monitor Manufactured in China for : Mindray DS USA, Inc. 800 MacArthur Blvd. Mahwah, NJ 07430 USA.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. d.b.a. Mindray North America
FDA (openFDA device enforcement)
Reported Dec 19, 2012
The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 5, 2012
IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Dec 5, 2012
Jimmy Dean French Toast & Sausage Sandwich, Net Wt 3.9 oz (110g); a food service individually butcher paper wrapped,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hillshire Brands Company
FDA (openFDA food enforcement)
Reported Dec 5, 2012
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Dec 5, 2012
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
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)
Reported Dec 5, 2012
NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ system is a semiconstrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Nov 28, 2012
The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Orthobiologics, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clinical Diagnostic Solutions
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic test for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2012
HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartsine Technologies, Limited
FDA (openFDA device enforcement)
Reported Oct 31, 2012
DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated Handpiece Catalog Number: 227305 The DePuy Mitek…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Hot Pepper Jelly, 4 and 8 ounce jars, labeled in part ***Jill's Jams & Jellies, Hampstead, MD 21074***
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hanover Pike Enterprises, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2012
Peanut Butter Bars Original: 3.0 oz, Two-Bar Box, UPC Code 837305005023, Manufactured by Sweet's Candy Company, Salt…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jer's Chocolates
4 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2012
Kraft Jalapeno String Cheese, Net Wt 12 Oz (340 g); a natural low-moisture part-skim mozzarella cheese with jalapeno…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 31, 2012
Label reads in part "*** ORGANIC Alden's ICE CREAM PEANUT BUTTER 'n CHIP 1.5 QTS ***" upc 0 72609 74191 2.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oregon Ice Cream, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2012
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2012
Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ethicon Endo-Surgery 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.