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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.

1,697 stored notices name Delaware, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Delaware too — those are in the archive.

Medical devices

Reported Aug 15, 2012

The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…

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

Radiometer America Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2012

TANGO3 Water Storage Tank with Ozone Disinfection System, Tango3, LLC, 132 Citizens Blvd., Simpsonville, KY 40067.…

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

Tango3 LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2012

PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…

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

Tripath Imaging, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2012

Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2012

Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 25, 2012

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…

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

Standard Process, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 25, 2012

Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use…

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

Terumo Cardiovascular Systems Corporation

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2012

superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…

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

superDimension, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 18, 2012

Oysters, IQF Standard, packed in 5 lb polyethlene bags, further packaged as 2 bags/box and 6 bags/box, and labeled in…

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

Wanchese Fish Company

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 18, 2012

Maryland Style Crab Soup 2340 Net Weight 4-4LBS. Winter Garden Quality Foods, Inc. 304 Commerce St. New Oxford, PA 17350

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

Winter Gardens Quality Foods Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 11, 2012

Rosati Cry Baby Sour Watermelon water ice, 6 fl oz

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

SR Rosati, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2012

Olympic Cool-Cap System is intended to provide treatment for neonatal hypoxic-ischemic encephalopathy (HIE). The…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Food

Reported Jun 27, 2012

Oskri, Peach Granola, Gluten Free, Nut Free, Dairy Free, Vegan, Halal, Kosher, Ingredients: Buck Wheat , Peaches 20%…

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

Oskri Organics Corp.

FDA (openFDA food enforcement)

Food

Reported Jun 20, 2012

Daufuski Brand boiled Oysters, 8 oz; Distributed by Liberty Gold Fruit, Inc.

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

Liberty Gold Fruit Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2012

The Brilliance iCT and iCT SP are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2012

T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the…

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

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2012

Vygon VY(TM)Flush Heparin Lock Flush Syringes, 1 Unit per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box…

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

Vygon Corporation

11 more products 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.