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 48,100 notices were distributed nationwide, so they reach Iowa too — those are in the archive.

Medical devices

Reported Oct 23, 2019

Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the…

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

Roche Diagnostics Operations, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2019

BD FACSLyric Flow Cytometer, 2-Laser 4 Color Instrument, REF: 662875, when using BD Trucount Tubes

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

Becton, Dickinson and Company, BD Biosciences

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 16, 2019

Madrona Market Delicatessen Hot Cocoa Mix, Net Wt. 2 lb (907 g), Distributed by Food Services of America, Inc.…

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

Diamond Crystal Brands Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 16, 2019

Clinical Chemistry, ABX Pentra Lipase CP, ABX Pentra 400/Pentrac400, REF: A11A01631, Model/Part # 1220001631, UDI #…

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

Horiba Instruments Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2019

20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product # RMS22606 - Product Usage: RMS HlgH-Flo…

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

Repro-Med Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2019

Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502

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

Roche Diagnostics Operations, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 16, 2019

Tep Say Crispy Tiny Shrimp Snack, Net Wt. 7 oz. in plastic jar UPC 7 37483 77926 9 Distributed By: First World Trading…

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

Vinh Sanh Trading Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal…

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

Howmedica Osteonics Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 9, 2019

Hy-Vee Mealtime Fried Rice in a 16 oz. black plastic container with clear plastic lid

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

Hy-Vee

FDA (openFDA food enforcement)

Medical devices

Reported Oct 9, 2019

Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all classes - Filling…

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

Voco GmbH

FDA (openFDA device enforcement)

Food

Reported Oct 9, 2019

Espinaler Razor Clams (Trimmed) 4/6 Classic Line, " N4R-LE7R printed on the tin AND/OR E7R MM/YYYY printed on the box.…

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

YTM, Inc. dba A Priori Specialty Foods

FDA (openFDA food enforcement)

Medical devices

Reported Oct 2, 2019

Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco system is used to make…

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

Elekta Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.

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

Abbott Nutrition, Division

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…

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

Allergan PLC

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC…

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

Danone Waters

FDA (openFDA food enforcement)

Food

Reported Sep 18, 2019

PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can

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

Natures One Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

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

Zimmer Biomet, Inc.

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…

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

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202

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

Becton Dickinson & Co.

1 more product in this recall

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.