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.

2,881 stored notices name Iowa, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Iowa too — those are in the archive.

Food

Reported Jun 15, 2022

Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.

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

The TJX Companies, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 8, 2022

BBU Fine Whole Wheat Flour Bulk-AA-50251, Bulk Tanker; SG Whole Wheat Fine Flour 2,000 lb. Tote-AA Storage instructions…

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

Ardent Mills, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 8, 2022

In-Line ventilator adaptor

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

Baxter Healthcare Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2022

BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically…

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

Becton, Dickinson and Company, BD Biosciences

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2022

Resin UPDATE CD-ROM, REF: 250-3020 inside VARIANTnbs Sickle Cell Program Reorder Pack, REF: 250-3000

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 8, 2022

JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…

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

The JM Smucker Company LLC

23 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 8, 2022

Jason & Mary Large Milk Peanut Butter Cup

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

Walnut Creek Chocolate Co. Inc.

14 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 1, 2022

Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…

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

Medtronic Neuromodulation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

KWIK-STIK" plus: Clostridium perfringens

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…

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

Teleflex Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

MicroScan WalkAway-40 plus Instrument REF B1018-283

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

Beckman Coulter Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113,…

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

Total Resources Intl

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…

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

Daavlin Distributing Company

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case

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

Eastland Food Corporation

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

HemosIL ReadiPlasTin, Part No. 0020301400

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

Instrumentation Laboratory

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model…

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

Proterixbio

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143

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

Simplivia Healthcare Ltd.

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038

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

Snak King Corporation

FDA (openFDA food enforcement)

Medical devices

Reported May 11, 2022

K-Wire, 1.35 mm x 170 mm

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.

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

Carl Zeiss Meditec AG

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.