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 Oct 7, 2026Updated Oct 13, 2026

Computed Tomography X-ray System, Model: uCT 530 with software

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

Shanghai United Imaging Healthcare Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…

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

Becton, Dickinson and Company

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

Lions Eye Bank Of Nebraska

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve

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

Ventec Life Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Halyard IV START KIT NON-STERILE REF: KRIV26-02

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

AVID Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

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

Bard Access Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

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

Happiest Baby, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Plum administration sets

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

ICU Medical, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Sep 23, 2026

Intercon Foaming Pear Hand Soap With Aloe, 28.7 fl. oz., Manufactured for: Intercon Chemical Company 1100 Central…

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

Intercon Chemical Co.

5 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Philips Patient Information Center iX REF:866389

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

Philips North America

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM

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

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

Rice & Bean Burrito. Ingredients: Rice, Refried Beans, Black Beans, Flame Roasted Corn, Pico De Gallo, Cheese. Net Wt:…

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

Taylor Fresh Foods Inc.

24 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7,…

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

Halyard IV Start Kit Non-Sterile REF: KRIV26-02

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

AVID Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…

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

C.R. Bard Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit)…

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

AVID Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS

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

Baxter Healthcare Corporation

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor…

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

Diagnostica Stago, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 9, 2026Updated Sep 16, 2026

Food to Live brand Organic Supergreens mix (kale, moringa leaf, wheat grass, & spirulina), 8 oz, 1 lb, 1.5 lb, 3 lb, 6…

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

Lexunder Inc.

FDA (weekly enforcement report)

Food

Reported Sep 2, 2026Updated Sep 7, 2026

bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961

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

Botticelli Foods, LLC

FDA (openFDA food enforcement)

Food

Reported Sep 2, 2026Updated Sep 13, 2026

Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…

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

Byron White Formulas, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 2, 2026Updated Sep 7, 2026

Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation

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

Merge Healthcare, Inc.

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.