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 Jun 8, 2022

In-Line ventilator adaptor

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

Baxter Healthcare Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2022

DYNEX Agility, Agility Analyzer, Model No. 67000

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

Dynex Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2022

The C304-HIS device features a guide wire to access the vein, a valve to reduce blood loss during the implant…

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Food

Reported Jun 8, 2022

JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…

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

The JM Smucker Company LLC

23 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…

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

Medtronic Neuromodulation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.

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

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Verigene Processor SP, Models 10-0000-07/10-0000-07R a component of the Verigene system

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

Luminex Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray

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

American Contract Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…

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

Certified Safety Mfg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…

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

Daavlin Distributing Company

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case

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

Eastland Food Corporation

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

HemosIL ReadiPlasTin, Part No. 0020301400

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

Instrumentation Laboratory

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143

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

Simplivia Healthcare Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2022

TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300…

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

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

TearCare version 1.0 SmartHubs

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

Sight Sciences, Inc.

FDA (openFDA device enforcement)

Food

Reported May 4, 2022

Organic Marketside Zucchini 2 Count packages/8 per case Ingredients: Organic Zucchini New WT. 6 oz. (170g) UPC:…

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

World Variety Produce Inc. dba Melissa's

FDA (openFDA food enforcement)

Medical devices

Reported Apr 27, 2022

4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010

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

Acumed LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 27, 2022

ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012,…

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

DNA Genotek Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 27, 2022

Carol's Cuts Cantaloupe Chunks Ingredients may include cantaloupe Prepared: Carols Cuts 1247 Argentine Blvd, KC KS…

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

Liberty Fruit Co. Inc. dba Carol's Cuts

3 more products in this recall

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.