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 Dec 7, 2022

Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC…

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

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

CMV IgM EIA, in vitro diagnostic.

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 7, 2022

Fudgeamentals Chocolate Fudge Bites (8 oz); packaged in clear plastic container

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

Fudgeamentals LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 7, 2022

GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel…

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

Greer Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

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

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2022

Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Canon Aplio ultrasound system, Model: Aplio i900 TUS-AI900, Aplio i800 TUS-AI800, Aplio i700 TUS-AI700, Aplio a550…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio…

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

iRhythm Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…

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

Medtronic MiniMed

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2022

Sedecal Soltus Battery Mobile X-Ray System REF Soltus 450 Battery Mobile X-Ray System REF Soltus 500

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

Sedecal Sa

FDA (openFDA device enforcement)

Medical devices

Reported Nov 9, 2022

BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are…

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

Becton, Dickinson and Company, BD Biosciences

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 9, 2022

Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6…

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

Bella Brands, LLC dba Bella Cucina Artful Food

13 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 9, 2022

Diana s Milk Chocolate Banana Babies UPC: 7-43490-00010-4 10.5-ounce 5 count packages

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

Diana's Bananas, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 9, 2022

Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP…

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

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 9, 2022

Food Club Chive Cottage Cheese, 16 oz; Hannaford Chive Cottage Cheese, 16 oz; Hood Chive Cottage Cheese, 16 oz and 24…

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

HP Hood LLC

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 2, 2022

da Vinci X (IS4200) and Xi (IS4000) systems, which consists of finished devices Surgeon Console (SSC), Patient Cart…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 2, 2022

THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14…

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

The Chai Box

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 2, 2022

GORE CARDIOFORM ASD Occluder. cardiovascular implant.

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 2, 2022

AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

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

ZOLL Circulation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 26, 2022

Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…

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

Abbott Vascular

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 26, 2022

Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…

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

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to…

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

Lyons Magnus LLC

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food 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.