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 Sep 6, 2023
Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2023
BioFire Respiratory Panel 2.1 (RP2.1), REF: 423742, For FILMARRAY systems, IVD, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
OEC Flexiview 8800 Systems with 9-inch Image Intensifier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Digisonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Jul 19, 2023
HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Medtronic Catalyft LS Expandable Interbody System, Anterier Standalone Cage, REF 981023322, spinal implant
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Great Value Sliced Strawberries. Item # 107356. Frozen, packaged flexible plastic bags. Net wt. 4 lbs (64oz). UPC on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oregon Potato Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 19, 2023
REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2023
BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
A20180 BATTER MIX X4 50.00 BAG
High riskUsing this product could cause serious injury, illness or death — stop using it now.Newly Weds Foods, Inc.
195 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quidel Cardiovascular Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Regal Gourmet Snacks Milk Chocolate Raisins 16oz. clear plastic tub, UPC 028744201002
High riskUsing this product could cause serious injury, illness or death — stop using it now.Regal Health Food International, Inc.
FDA (openFDA food enforcement)
Reported Jul 5, 2023
Access Hybritech p2PSA reagent, REF B03704 and REF A49752.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2023
DigitalDiagnost C90, Model No. 712034 and 712035
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Rudolphs OnYums Onion Flavored Snack Rings 3 oz. UPC 0-24622-57106-9 packaged in metallized film bags, 15 bags per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rudolph Foods Company
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
enterade Advanced Oncology Formula; Original Vanilla Flavor; Medical Food; Helps manage and maintain GI function; 8 FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Entrinsic Health Solution Inc.
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Serrated Blade Applicator Kit (12 Sample), REF: 552687, For use with the Spife Nexus system, Contents: 30 Blade…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
KARL STORZ Radel Sterilization Trays, Models: 27717A, 27717B, 39301A, 39301C, 39231XA, 39301C1, 39311A, 39317A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
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.