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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 27, 2017

Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…

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

Medtronic Navigation, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2017

Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2017

Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…

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

Mako Surgical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 13, 2017

MOSAIQ Medical Charged-Particle Radiation Therapy System

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 13, 2017

OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0…

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

Litehouse Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 13, 2017

Southeastern Mills, Biscuit Gravy Mix, Net Wt. 2.75oz (77g), 4.5oz (128g) flexible plastic packages.

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

Southeastern Mills Custom Seasoning Solutions

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 6, 2017

Michele s Toasted Muesli, 16 oz bags, 12 units per case

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

Michele's Granola LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2017

iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…

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

Optovue, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

IQF Green Beans, Keep Frozen. 11 varieties, packaged under the following brands and sizes: 1) Bountiful Harvest French…

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

Lakeside Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…

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

Cyberonics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic resonance scanner…

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

GE Medical Systems, LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Plum 360 Infusion System

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)

Medical devices

Reported Aug 16, 2017

Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…

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

International Medsurg Connection, Inc.

58 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aortic Arch Cannulae are…

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

Sorin Group USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2017

InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…

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

Quidel Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 2, 2017

1) Key Lime Dessert Cake, Grandma's Bake Shoppe, NET WT. 14 OZ. (400 g), UPC 8 24153 02582 2

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

Beatrice Bakery Co.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 230 V

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

Sorin Group USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2017

Agfa Healthcare NX 3.0.8950 Imaging Processing Software

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl,…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 19, 2017

Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…

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

Kroger Corporate Food Technology Laboratory

FDA (openFDA food enforcement)

Medical devices

Reported Jul 19, 2017

Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…

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

Natus Neurology Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…

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

Oscor, Inc.

1 more product 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.