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.

Medical devices

Reported Feb 21, 2024

global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2024

Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…

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

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2024

3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Sperm separation media are used to separate motile sperm from other constituents of semen.

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

Fujifilm Irvine Scientific, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 7, 2024

Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT…

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

Covidien LP

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

Rizo Bros Cotija (Grated) 8 oz. UPC 72724200043 7 oz. UPC 7-27242-14022-5 Tio Francisco, Casa Cardenas 9 oz. UPC…

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

Rizo Lopez Foods, Inc. dba Don Francisco Cheese

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2024

Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25

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

Vortex Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

Snapshot NIR, REF: KD204

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

Kent Imaging, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Pan de Racho (Feria), Net Wt. 2lbs, individually packaged in clear plastic bag.

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

Lara's Bakery 3 LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002

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

Ossur H / F

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.

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

St. Jude Medical, Atrial Fibrillation Division, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Vermont Village Unsweetened Apple Sauce (24oz)

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 24, 2024

FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System

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

Abbott Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2024

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2024

VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, non-ridged.

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 24, 2024

Ministry of Snacks Sweet and Savory Collection #8700

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

Houdini Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 24, 2024

Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken…

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

TreeHouse Foods, Inc.

14 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer…

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

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

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.