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.
Reported Oct 5, 2022
Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DICOM Grid, Inc. d/b/a Ambra Health
FDA (openFDA device enforcement)
Reported Oct 5, 2022
HyVee Oven Baked Beans in 16 OZ plastic containers (UPC 0075450500640, 12 retail units per case)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hy-Vee, Inc. dba Hy-Vee Fresh Commissary
FDA (openFDA food enforcement)
Reported Oct 5, 2022
MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Oct 5, 2022
t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 28, 2022
ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Muktanand Foods Inc.
FDA (openFDA food enforcement)
Reported Sep 21, 2022
MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 21, 2022
Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Steris Corporation Hopkins Facility
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Various Angiography packs/trays
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2022
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Optikgeraete GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2022
(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2022
HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Aug 24, 2022
Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Albertsons Companies LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2022
ARIES SARS-CoV-2 Assay
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Aug 17, 2022
The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neotract Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Amaranth Grain Organic, brand Natural Grocers, packaged in plastic bag, net wt. 1 LB (454g) UPC 0 00080 12550 1. Label…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitamin Cottage Natural Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Aug 3, 2022
REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
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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.