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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 Jun 4, 2025

VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges, of 18 slides per cartridge, for a total of…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 4, 2025

Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2025

Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8"…

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

C.R. Bard Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 21, 2025

Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour…

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

Meddev Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 14, 2025

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported May 14, 2025

Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz., in clear plastic clamshell container, UPC 00773164

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

Taylor Farms Illinois Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 7, 2025

Enhanced Verify Evaluation Handset (CFN HH90130FA)

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2025

Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or…

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

Spectrum Medical Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software…

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

Abbott Laboratories

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED,…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly

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

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product…

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

Avanos Medical, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…

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

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

t:slim X2 Insulin Pump with Interoperable Technology

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

Tandem Diabetes Care, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with…

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

Thoratec LLC

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2025

BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.

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

Tristar Food Wholesale Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 16, 2025

Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072…

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

Qapel Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Apr 9, 2025

Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…

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

Nestle-USA, Inc. (Corporate Office)

2 more products in this recall

FDA (openFDA food 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.