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 Jul 24, 2019

Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2019

White Cheddar 5906-KD is a non-GMO White Cheddar Cheese Blend dried cheese powder. Product was shipped in bulk bags,…

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

Commercial Creamery Company

FDA (openFDA food enforcement)

Food

Reported Jul 24, 2019

Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt. 7 3/4 OZ. UPC Code 2840063242

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

Frito-Lay, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2019

Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…

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

Medline Industries, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2019

Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit

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

Wilton Brands

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2019

Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena…

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

Helena Laboratories, Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent, Product Number HY0305Z

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

Madison Polymeric Engineering

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.

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

Roche Diagnostics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2019

WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…

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

UNFI General Corporate

FDA (openFDA food enforcement)

Medical devices

Reported Jun 26, 2019

Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…

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

Cytocell Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1 Product Code: X425H Product Usage: ETHIBOND…

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

Ethicon, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 26, 2019

Maglio Companies Jalapeno Peppers sold in the following sized packages: 10 lb. Qdoba Pepper; 1-1/9 BU Pepper, Jalapeno…

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

The Fresh Group, Ltd.

FDA (openFDA food enforcement)

Food

Reported Jun 19, 2019

Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Sandwich. Horchata Rice Milk & Cinnamon frozen dessert…

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

Coolhaus

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam…

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

Skytron, Div. The KMW Group, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…

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

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Horizon Cardiology Hemo

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

Change Healthcare Israel Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US

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

Dole Fresh Vegetables

1 more product in this recall

FDA (openFDA food 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.