All recall categories

Recalls distributed in Nebraska

These notices name Nebraska 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.

2,352 stored notices name Nebraska, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Nebraska too — those are in the archive.

Medical devices

Reported Aug 21, 2019

Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452

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

Luminex Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2019

SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System

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

Pega Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2019

Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…

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

Wismettac Asian Foods, Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2019

Maximum Pelvic Trainer (MPT)

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

Ralston Group

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2019

ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2019

The Grinch Sugar Cookie Mix with Sprinkles, 22.3 oz glass jar, 6/case

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

Brand Castle LLC

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2019

Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100

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

Medela Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2019

Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1

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

Merge Healthcare, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2019

Ragu Chunky Sauce Tomato, Garlic & Onion 45oz and 66oz retail sizes sold in plastic jars

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

Mizkan America, Inc. - Corporate

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 31, 2019

Great Value Chopped Spinach, packed in poly bags, net wt. 12 oz. 12 oz. bag UPC: 0 78742 23740 4. master case UPC: 3 00…

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

National Frozen Foods Corporation

FDA (openFDA food enforcement)

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

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)

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 17, 2019

Cios Alpha VA20/ VA30 mobile X-Ray systems

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2019

Signature Select Avocado Chunks, 12 oz. (340 g) Stand-up pouch Re-sealable, Keep Frozen; UPC 2113009412 Ingredient:…

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

Nature's Touch Frozen Foods (West)

FDA (openFDA food enforcement)

Medical devices

Reported Jul 10, 2019

Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT)…

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 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 Jul 10, 2019

DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…

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

Zimmer Biomet, Inc.

2 more products 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)

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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.