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 25, 2013
Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is an in vitro diagnostic test intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2013
HyVee Chocolate Caramel Clusters, packaged in 9-oz. clear plastic clamshell containers (UPC 077232125153), 16…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Palmer Candy Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
Crunch Pak Apple Slices with Low Fat Caramel Dip, 5/2.5 oz. Tart with Caramel Sauce. The clamshell includes 5/2 oz.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Crunch Pak, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Healthcare It
FDA (openFDA device enforcement)
Reported Dec 11, 2013
Product #4124: Caramel dip in plastic containers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gold Medal Products
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
Woodstock Frozen Organic Pomegranate Kernels are sold in 8 oz. (227 gram) re-sealable plastic pouches with the UPC 0…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Scenic Fruit Co.
FDA (openFDA food enforcement)
Reported Dec 4, 2013
Baxter, VIAL-MATE Adaptor, 2B8071, Rx Only, STERILE R, Baxter Healthcare Corporation, Deerfield, IL 30015 USA The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Dec 4, 2013
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2013
Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
7 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 4, 2013
2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recess 12 MM Fixation of fractures, osteotomies, nonunions,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…
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)
Reported Nov 27, 2013
ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ivoclar Vivadent, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
36 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to visualize upper airway and aid in placement of tracheal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY; Terri Lynn Inc.; Deluxe Mixed; No Peanuts; NET WT. 16 OZ.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Terri Lynn Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 20, 2013
Digestive Enzymes, 60 Capsules/Bottle under the following brand names: 21st Century Digestive Enzymes, 60…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.21st Century Healthcare, Inc.
FDA (openFDA food enforcement)
Reported Nov 20, 2013
Carestream Vue PACS; VIRTUAL ACCESS SOFTWARE, WORKGROUP The CARESTREAM PACS is an image management system whose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health Inc.
49 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.), AW VolumeShare 5 (AW VOLUMESHARE 5 WITH ANGIOVIZ OPTION), AW Server.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Composite Series Skull Clamp, one clamp per tote. The MAYFIELD¿ Skull Clamp (A3059) is a cranial stabilization device,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Artis zee systems x-ray, angiographic system
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)
Reported Nov 20, 2013
Acetabular Pressurizer; single use and six units per box. The Acetabular Pressurizer 0206-522-000 is an accessory to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
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.