All recall categories

Recalls distributed in Delaware

These notices name Delaware 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.

1,727 stored notices name Delaware, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Delaware too — those are in the archive.

Medical devices

Reported Jul 16, 2014

Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jul 16, 2014

Oaxaca brand of Anelina in 1/2 oz plastic bags with paper label reading in part: "Oaxaca Mexican Products 100 8th…

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

Oaxaca Mexican Products

FDA (openFDA food enforcement)

Food

Reported Jul 16, 2014

Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…

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

Oregon Freeze Dry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure…

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

RGI Medical Manufacturing, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…

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 Jul 16, 2014

Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)

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

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

GE Healthcare, Compact Airway Modules E-CO, E-COV, E-COVX, E-CAiO, E-CAiOV and E-CAiOVX. The Datex-Ohmeda S/5MT Compact…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

APTIMA Urine Collection Kit; Catalog Number 301040, Lots 27231, 27232, 27233, and 27234. Product Usage: The APTIMA…

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

Gen-Probe Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive (BioGlue) is indicated for use as an adjunct to…

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

CryoLife, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 11, 2014

Greens+ Vegan Crisp Bars - Dark Chocolate Almond Blueberry in 1.4 oz packages.

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

Orange Peel Enterprises, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 28, 2014

LATEX-FREE; EXTENSION SET; For Bladder Irrigation or Urinary Drainage, Compatible with T-U-R FLOW-POUCH RESERVOIR, list…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 28, 2014

Lipton Pure Leaf Iced Tea Unsweetened 18.5OZ PL 6 Pack and 12 Pack

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

Pepsi Beverages Company

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 28, 2014

SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket; used with the Equator Convective Warmer, are intended…

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

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Food

Reported May 28, 2014

Stonyfield YoBaby Pear/Peach Organic Whole Milk Yogurt multipack- 6 pack plastic cups- 3 peach and 3 pear/4 oz each…

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

Stonyfield Farm

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 21, 2014

Fresh Express, Italian, Crunchy Romaine Lettuce and Red Cabbage Salad, 10oz clear plastic bags, UPC: 71279-21100.

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

Chiquita Brands International, Inc.

FDA (openFDA food enforcement)

Food

Reported May 21, 2014

TRADER GIOTTO'S CAESAR SALAD with Caesar Dressing, NET WT. 8/5 OZ (241g).

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

H Group

FDA (openFDA food enforcement)

Medical devices

Reported May 21, 2014

HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a…

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

HeartWare Inc.

FDA (openFDA device enforcement)

Food

Reported May 14, 2014

Bissinger's Dark Chocolate Bunny Ears, 1 oz, individually wrapped in clear plastic with an ingredient card insert and…

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

Karl Bissinger LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 7, 2014

Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…

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

Hospira Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…

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

BioMerieux SA

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104,…

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

HeartWare Inc.

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.