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 5, 2024

BD Pyxis MedStation ES, REF: 323, Medication Cabinet

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

CareFusion 303, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

FDR Visionary Suite - Intended to generate digital or conventional radiographic images of the skull, spinal column,…

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

FUJIFILM Healthcare Americas Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2024

Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0075450486740, 6 containers per case. Hy-Vee Cookies & Cream…

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

Hy-Vee Stores Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2024

Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 Trevo XP ProVue…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2024

Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number:…

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

Channel Medsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2024

SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Food

Reported May 29, 2024

chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g

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

Kairo's Group, Inc. dba Chuao Chocolatier

FDA (openFDA food enforcement)

Medical devices

Reported May 22, 2024

Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US

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

Fisher & Paykel Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2024

HeartSine samaritan PAD (Public Access Defibrillator), Type: SAM 350P, SAM 360P, SAM 450P

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2024

LASER Application Instrument, 23 cm, REF: 8694; LEUNIG-GREVERS LASER Application, REF: 461000

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,

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

Allergan Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly

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

Thoratec Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported May 1, 2024

Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2024

Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

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

Parker Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests

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

Quidel Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only,

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

Masimo Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2024

Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2024

LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Food

Reported Apr 17, 2024

Onion Yellow Med 3 Outer Rings 4-5 LB in a 5 LB ,vacuum sealed, clear plastic bag. Labeling: White paper label with the…

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

Pueblo Fruits, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 17, 2024

Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Electrolytic tin-plated cans, with paper label. 12-pack case…

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

Whitley Peanut Factory, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 10, 2024

ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.

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

Abbott Laboratories

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.