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 Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.

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

Smith & Nephew Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the…

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

Abbott Medical

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2024

Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032

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

Curio Spice Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients who would benefit from a suction pump (NPWT), as it may…

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

Smith & Nephew Medical, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog Number: Z-800WF. The Z-800 Infusion system is…

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

Zyno Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component:…

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

Draeger Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…

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

Olympus Corporation of the Americas

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 20, 2024

raw, yellow onions (sliced, diced, slivered, ringed), intended for food service, packaged in plastic bags

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

Taylor Farms Colorado, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 20, 2024

Home Chef Chicken Street Taco, Net Wt. 9.93 oz, packaged in a plastic tray with clear plastic lid, perishable item kept…

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2024

SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic…

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

Shimadzu Corporation Medical Systems Division

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Abbott Alinity m HPV AMP Kit, used with the Alinity m System, product codes: a) REF 09N15-095; b) REF 09N15-090; c) REF…

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

Abbott Molecular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.

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

Danone US LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 Forehead Probe, Adult,…

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

Nihon Kohden America Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to…

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

Percussionaire Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

remel BactiDrop Acridine Orange, REF 21502, 50 per package.

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

Remel, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Item 407118, UPC 13454 38493, Bistro 28 Creamy Green Chile Chicken Enchilada Express Meal Kit. Make 6 Enchiladas. Ready…

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

Reser's Fine Foods, Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

Brand Name: Vial2Bag Advanced¿ Product Name: Vial2Bag Advanced¿ 20mm Admixture Device Model/Catalog Number: 6070030…

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

West Pharmaceutical Services AZ, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

1) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The…

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

Westmed, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2024

Lactaid Lactose Reduced milk 1. 96 oz Lactaid Whole Milk 2. 96 oz Lactaid 2% Milk 3. 96oz Lactaid 1% Milk 4. 96oz…

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

HP Hood LLC

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.