The Recall Desk

State

Nebraska product recalls

73,817 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,580
Critical
713
Severe
1,345
Most recent
2026-10-28

Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50051–50075 of 78397

  • HighFDA (Devices)·Z-2758-2016·2016-09-14

    Siemens e.cam and Symbia E Gamma Camera Patient Bed Recall

    Siemens is recalling e.cam and Symbia E gamma camera systems because patient hair can become caught in the patient bed drive mechanism.

    Product
    e.cam and Symbia E gamma camera systems with patient beds To detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2727-2016·2016-09-14

    Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm

    Hospira Inc. is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and delay or interrupt therapy.

    Product
    Plum A+ Infusion Pump with Hospira MedNet Software. List Number 20792. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V664000·2016-09-14

    Thomas Built Buses Saf-T-Liner C2 Recall for Brake Indicator Error

    Daimler Trucks is recalling 2016-2017 Thomas Built Buses Saf-T-Liner C2 school buses because the brake malfunction light may display "PARK" instead of "BRAKE," increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1483-2016·2016-09-14

    Amerisource Recalls Mispackaged Amphetamine Tablets Due to Unit Dose Errors

    Amerisource Health Services is recalling 1,416 cartons of 15 mg amphetamine tablets because blister cavities may contain more than one tablet.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 15 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2760-2016·2016-09-14

    Invivo Xper Flex Cardio Patient Monitoring System Recalled for Frozen Display

    Invivo Corporation is recalling Xper Flex Cardio Patient Monitoring Systems because SpO2 and NIBP measurements may freeze on the display.

    Product
    The system provides the ability to transmit patient data files for storage, viewing and analysis at distributed locations via the intranet or Internet, or may function as a stand-alone device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1486-2016·2016-09-14

    Amerisource Health Services Recalls Mispackaged Amphetamine Extended-Release Capsules

    Amerisource Health Services is recalling 834 cartons of amphetamine extended-release capsules because blister cavities may contain more than one tablet or capsule.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 10 mg 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2733-2016·2016-09-14

    Integra Cranial Access Kits Recalled Due to Potential Sterility Compromise

    Integra LifeSciences is recalling Cranial Access Kits because product seals may open during distribution, rendering the devices unsterile.

    Product
    Integra Cranial Access Kits, Catalogue Nos. INSHITH; INSHITHRZN; INSHITHND
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2746-2016·2016-09-14

    Maquet Operating Room Table Connecting Bracket Recall for Welded Joint Failure

    Maquet is recalling Connecting Bracket (Fixture) Devices because post-market surveillance reports indicate the welded joint between the square mount and the first fixable swivel joint is broken.

    Product
    The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element to support ancillary head rests on a Maquet operating room table immediately before, during and after surgical interventions as well as for examination and treatment. The fixture is used to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2067-2016·2016-09-14

    Nature Made Multi + Omega-3 Recalled for Possible Salmonella Contamination

    Pharmavite is recalling specific lots of Nature Made Multi + Omega-3 supplements due to possible Salmonella contamination. Consumers should stop using the affected products.

    Product
    Nature Made(R) Multi + Omega-3, 150 count, UPC 0-31604-04173-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2079-2016·2016-09-14

    Lysander's Premium Teriyaki Marinade Recalled for Undeclared Allergens

    Geneva Foods is recalling Lysander's Premium Teriyaki Marinade because it contains undeclared soy, wheat, and sulfites.

    Product
    Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 units per case. Manufactured by Geneva Foods, LLC.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2725-2016·2016-09-14

    Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm

    Hospira is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.

    Product
    Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1484-2016·2016-09-14

    Amerisource Health Services Recalls Mispackaged Amphetamine Tablets

    Amerisource Health Services is recalling 867 cartons of 20 mg amphetamine tablets due to unit dose blister cavities containing more than one tablet.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2081-2016·2016-09-14

    Lysander's Bourbon Flavor Rub Recalled for Undeclared Allergens

    Geneva Foods is recalling Lysander's All Natural Bourbon Flavor Rub because it contains undeclared soy, wheat, and sulfites.

    Product
    Lysander's All Natural Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g), foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2066-2016·2016-09-14

    Nature Made Adult Gummies Multi Recalled for Possible Salmonella Contamination

    Pharmavite is recalling specific lots of Nature Made adult gummies Multi due to possible Salmonella contamination. Consumers should check lot numbers and expiration dates.

    Product
    Nature Made(R) adult gummies Multi, 150 count, UPC 0-31604-04172-4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2071-2016·2016-09-14

    Nature Made Super B-Complex Recalled for Possible Bacterial Contamination

    Pharmavite is recalling Nature Made Super B-Complex vitamins due to possible Staphylococcus aureus and Salmonella contamination in specific lots.

    Product
    Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 460 count, UPC 0-31604-02728-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2072-2016·2016-09-14

    Nature Made Super B-Complex Recalled for Possible Bacterial Contamination

    Pharmavite is recalling Nature Made Super B-Complex supplements due to possible Staphylococcus aureus and Salmonella contamination in specific lots.

    Product
    Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 360 count, UPC 0-31604-02729-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2765-2016·2016-09-14

    Hologic Recalls SureSight Obturator Introducer Systems Due to Tip Breakage

    Hologic is recalling 1,440 SureSight Obturator Introducer Localization Systems because the tip may break at the glue joint.

    Product
    SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI. ILS-0914-20-OB (9G Introducer Localization Set (OB Model) for ATEC0914-20MR Handpiece)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2737-2016·2016-09-14

    Philips BrightView XCT Upgrade Recalled for Potential Patient Contact

    Philips is recalling three BrightView XCT Upgrade units due to a software defect that may cause the detector to contact patients during specific scans.

    Product
    BrightView XCT Upgrade Model 882454
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2729-2016·2016-09-14

    Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm

    Hospira Inc. is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.

    Product
    Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2738-2016·2016-09-14

    Terumo Recalls Pinnacle Introducer Sheaths Due to Valve Leakage

    Terumo Medical Corporation is recalling Pinnacle Introducer Sheaths due to a manufacturing issue causing valve leakage, which poses a risk of incremental blood loss.

    Product
    PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2762-2016·2016-09-14

    Riverpoint Medical Recalls Webglo Polypropylene Surgical Sutures Due to Seal Issues

    Riverpoint Medical is recalling specific lots of Webglo polypropylene surgical sutures because the seals may open during distribution or packaging.

    Product
    Polypropylene Surgical Sutures, brand Webglo, for vet use. Product is sterile. Part number: GP8665 Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2763-2016·2016-09-14

    Blackrock NeuroPort Biopotential Signal Processing System Recall for Labeling Error

    Blackrock Microsystems is recalling 81 Neural Signal Amplifiers because the device and patient cable are incorrectly labeled as Type CF Applied Parts.

    Product
    Neural Signal Amplifier. Part Numbers: 4208, 5703, 5749, 5748, 5747. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes. Biopotential signals include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2074-2016·2016-09-14

    Nature Made Hair Skin Nails Gummies Recalled for Microbial Count

    Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.

    Product
    Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC 0-31604-04132-8-1
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2764-2016·2016-09-14

    Blackrock NeuroPort Patient Cables Recalled for Incorrect Labeling

    Blackrock Microsystems is voluntarily recalling 120 Patient Cables because they are incorrectly labeled as Type CF Applied Parts.

    Product
    Patient Cable. Part Numbers: 4460, 6735. Sterile within Chipboard Boxes within corrugated cartons. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes.…
    Category
    Medical Device
    Distribution
    Distributed nationwide