The Recall Desk

State

Nebraska product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45301–45325 of 78389

  • CriticalFDA (Drugs)·D-0963-2017·2017-07-19

    ZRECT Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling ZRECT Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    ZRECT Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 852675999451
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2539-2017·2017-07-19

    Wildway Apple Cinnamon Granola Recalled for Listeria Contamination Risk

    Wildway LLC is recalling specific lots of Apple Cinnamon Grain-Free Granola due to potential Listeria monocytogenes contamination.

    Product
    Wildway Apple Cinnamon Grain-Free Granola 8 oz and 10 oz UPC: 85866005190 and UPC: 864352000015 packaged in plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0956-2017·2017-07-19

    Advanced Pharma Recalls Potassium Phosphate Injection Due to Sterility Concerns

    Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate Injection due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 15 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-922-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2540-2017·2017-07-19

    Wildway Banana Nut Granola Recalled for Listeria Contamination Risk

    Wildway LLC is recalling 434 cases of Banana Nut Grain-free Granola due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Wildway Banana Nut Grain-free Granola 8 oz. UPC: 858660005176 packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2576-2017·2017-07-19

    Wildway LLC Recalls Trader Joe's Grainless Granola Due to Listeria Risk

    Wildway LLC is recalling specific lots of Trader Joe's Grainless Granola due to potential contamination with Listeria monocytogenes.

    Product
    Trader Joe's Grainless Granola 8 oz. (SKU 56307) packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2542-2017·2017-07-19

    Wildway Vanilla Bean Espresso Granola Recalled for Listeria Risk

    Wildway LLC is recalling 442 cases of Vanilla Bean Espresso Grain-free Granola due to potential Listeria monocytogenes contamination.

    Product
    Wildway Vanilla Bean Espresso Grain-free Granola 8 oz. UPC: 858660005206 packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2340-2017·2017-07-19

    Oscor ATAR Reusable Extension Cables Recalled for Connector Separation Risk

    Oscor, Inc. is recalling ATAR Reusable Extension Cables because they may separate from the connector during use, posing a risk to patients.

    Product
    ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series. Model codes: 53912 - MDTS ATAR REUSABLE, 53912A - MDTS ATAR REUSABLE, ATAR MDTS REUSABLE, ATAR-A DARK BLUE REUSABLE, ATAR-MDT REUSABLE, ATAR-MDT2…
    Category
    Medical Device
    Distribution
    39 states
  • SevereFDA (Drugs)·D-0957-2017·2017-07-19

    Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns

    Baxter Healthcare is recalling 0.9% Sodium Chloride Injection bags due to customer complaints about leaking bags, which raises concerns about the product's sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0960-2017·2017-07-19

    Teva Recalls Paliperidone Extended-Release Tablets Due to Dissolution Failure

    Teva Pharmaceuticals is recalling 360 bottles of Paliperidone Extended-Release Tablets because one tablet failed a routine stability test for drug release.

    Product
    Paliperidone Extended-Release Tablets, 3 mg, 90 count bottles, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA, NDC: 0591-3693-19
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0972-2017·2017-07-19

    Baxter Recalls 5% Dextrose Injection Due to Sterility Concerns

    Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2733-2017·2017-07-19

    Oscor ATAR Disposable Extension Cables Recalled for Connector Separation Risk

    Oscor, Inc. is recalling ATAR Disposable Extension Cables because they may separate from the connector during use, posing a risk to patients.

    Product
    ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI Disposable Series. Model codes: ATAR D-A DARK BLUE DISPOSABLE, ATAR D-V WHITE DISPOSABLE, ATAR D-MDT DISPOSABLE, ATAR D-T DISPOSABLE, ATAR D-R DISPOSABLE…
    Category
    Medical Device
    Distribution
    39 states
  • SevereFDA (Drugs)·D-0959-2017·2017-07-19

    Bristol-Myers Squibb Recalls Eliquis 5mg Tablets Due to Labeling Error

    Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.

    Product
    EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and Pfizer Inc. New York, NY 10017 USA, NDC 0003-0894-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V450000·2017-07-19

    Daimler Trucks Recalls 2017-2018 Freightliner and Western Star Trucks for Fuel Pump Defect

    Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.

    Product
    FREIGHTLINER CUSTOM CHASS — FREIGHTLINER CUSTOM CHASS, FREIGHTLINER, WESTERN STAR XCP, 122SD, 6900, XCM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0953-2017·2017-07-19

    Advanced Pharma Recalls Succinylcholine Chloride Injection Due to Sterility Concerns

    Advanced Pharma Inc. is recalling QUELICIN (Succinylcholine Chloride) Injection due to a lack of assurance of sterility. The recall affects 2,350 units distributed nationwide.

    Product
    QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC 15082-814-79), c) 10mL vial (NDC 15082-814-61), Repackaged by Advanced Pharm, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0954-2017·2017-07-19

    Advanced Pharma Recalls Potassium Phosphate IV Bags Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 72 units of Potassium Phosphate IV bags nationwide due to a lack of assurance of sterility.

    Product
    Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 20 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-926-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0955-2017·2017-07-19

    Advanced Pharma Recalls Potassium Phosphate Bags Due to Sterility Concerns

    Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.

    Product
    Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 30 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-924-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2705-2017·2017-07-19

    O-Two Adult Ventilation Timer Recalled Due to Flash Rate Malfunction

    O-Two Medical Technologies is recalling Adult Ventilation Timers because the flash rate may be twice the labeled rate, potentially affecting ventilation guidance.

    Product
    O-Two Adult Ventilation Timer, MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 --- INTENDED USE: The Adult Ventilation Timer is intended to guide the rescuer to provide ventilations at a rate appropriate for adult patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2729-2017·2017-07-19

    Natus Neurology Recalls Elite 5 MHz Vascular Probes Due to Noise Issues

    Natus Neurology is recalling 2,335 Elite 5 MHz Vascular Probes because excessive background noise may mask heart rate and blood flow signals.

    Product
    Nicolet¿ Elite¿ 5 MHz Vascular Probe, Model #: X1L004, Catalog Code: N500. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Devices)·Z-2695-2017·2017-07-19

    St. Jude Medical Recalls Infinity 7 Implantable Pulse Generators

    St. Jude Medical is recalling 373 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices may cause a loss of neuromodulation therapy.

    Product
    Infinity 7, Implantable Pulse Generator, REF 6662, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2679-2017·2017-07-19

    ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption

    ICU is recalling Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose 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 based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2694-2017·2017-07-19

    St. Jude Medical Recalls Infinity 5 Implantable Pulse Generators

    St. Jude Medical is recalling 54 Infinity 5 Implantable Pulse Generators due to a risk of therapy loss if exposed to monopolar electrosurgical devices.

    Product
    Infinity 5, Implantable Pulse Generator, REF 6661, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2731-2017·2017-07-19

    O-Two Medical Recalls Burn Relief Dressings Due to Sterilization Concerns

    O-Two Medical Technologies is voluntarily recalling specific lots of Burn Relief hydrogel dressings because there is a lack of evidence validating the sterilization dose, posing a potential contamination risk.

    Product
    Burn Relief¿, MODEL #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200, CATALOG #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200 --- DRESSING,WOUND,HYDROGEL W/OUT DRUG AND/OR BIOLOGIC. --- Burn Relief¿ products are self-cooling, non-adhering and are intended to be used on 1st and 2nd…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2696-2017·2017-07-19

    St. Jude Medical Recalls Infinity 7 Implantable Pulse Generators

    St. Jude Medical is recalling 40 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices during medical procedures may cause a loss of neuromodulation therapy.

    Product
    Infinity 7, Implantable Pulse Generator, REF 6663, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
    Category
    Medical Device
    Distribution
    Distributed nationwide