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.

2,383 stored notices name Nebraska, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Nebraska too — those are in the archive.

Medical devices

Reported Apr 1, 2026

BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers:…

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

I.T.S. GmbH

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…

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

Merit Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2026

SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED…

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

Savannah Bee Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

DxC 700 AU, REF: B86444, B86446

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

Beckman Coulter Mishima K.K.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Artelon FlexBand Dynamic Matrix Ref: 31057

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

International Life Sciences

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2026

VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***)…

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

Palmetto Gourmet Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2026

PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART…

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

Raz Design Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2026

Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software…

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

Aesculap Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2026

Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…

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

Vascutek, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with…

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

MRIMed Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2026

Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case

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

Sb Food LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…

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

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 25, 2026

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid…

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

Pure Solutions, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…

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

Stryker Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 19, 2026

Sobico USA LLC Recalls Siluriformes Fish Products Imported Without The Benefit of Import Reinspection

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

Sobico USA LLC

USDA FSIS

Food

Reported Feb 18, 2026

Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc.,…

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

Domino Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 18, 2026

Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…

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

McCain Foods USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 18, 2026

CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET…

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

Ventura Foods LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…

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

Beckman Coulter, Inc.

1 more product 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.