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 Sep 23, 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.

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 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 (weekly enforcement report)

Medical devices

Reported Sep 23, 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 (weekly enforcement report)

Medical devices

Reported Sep 23, 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 (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Plum administration sets

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

ICU Medical, Inc.

7 more products in this recall

FDA (weekly enforcement report)

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, 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 (weekly enforcement report)

Food

Reported Sep 23, 2026

Diced Jalapenos. Ingredients: Jalapeno Pepper. Net Wt: 3.75 oz. Keep Refrigerated. Distributed by: Taylor Farms Inc.,…

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 (weekly enforcement report)

Medical devices

Reported Sep 16, 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 (weekly enforcement report)

Medical devices

Reported Sep 16, 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 (weekly enforcement report)

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

19 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)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…

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

Covidien, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200…

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

Kico Knee Innovation Company

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

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

Paragonix Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

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

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

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

SDI Limited

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2026Updated Sep 7, 2026

Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with…

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

529 Commerce, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2026Updated Sep 7, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

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

Erbe USA 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.