The Recall Desk

State

Nebraska product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34326–34350 of 78317

  • ModerateFDA (Drugs)·D-1865-2019·2019-09-25

    Aurolife Pharma Recalls Allergy Relief Tablets Due to Impurity Failures

    Aurolife Pharma is recalling specific lots of Allergy Relief (Fexofenadine Hydrochloride) 180 mg tablets because they failed impurities and degradation specifications.

    Product
    Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53); b) 30-count cartons (NDC 60000-409-30); c) 45-count bonus cartons (NDC 60000-409-48); d) 45-count cartons (NDC 60000-409-45); CAREone, Distributed by: Foodhold…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2545-2019·2019-09-25

    CooperSurgical Recalls LEEP Return Patient Pads Due to Expiration Date Errors

    CooperSurgical is recalling LEEP Return Patient Pads because the expiration dates on the outer boxes have the month and day reversed compared to the individual pouches.

    Product
    LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V676000·2019-09-23

    Mercedes-Benz Recalls E-Class Wagons Due to Rear Spoiler Detachment Risk

    Mercedes-Benz is recalling specific 2017-2019 E-Class wagons because the rear spoiler may detach while driving, creating a road hazard and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, E63S, E 400, E400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V674000·2019-09-23

    Spartan Metrostar and Gladiator Recall for Air Brake Control Line Defect

    Spartan is recalling 2004-2020 Metrostar and Gladiator vehicles because unprotected air brake control lines may cause unexpected brake application and increase crash risk.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V673000·2019-09-23

    Pleasure Way Recalls 2018-2020 Motorhomes for Awning Drive Mechanism Failure

    Pleasure Way is recalling 2018-2020 Plateau, Ascent, and Lexor motorhomes because the awning drive mechanism may fail, causing the awning to extend unexpectedly.

    Product
    PLEASURE WAY — PLEASURE WAY PLATEAU, LEXOR, ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V668000·2019-09-20

    Forest River Recalls 2020 Cherokee Trailers Due to Wiring Exposure

    Forest River is recalling 2020 Cherokee trailers because missing protective paneling exposes distribution panel wiring, increasing the risk of electrical shock or fire.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V675000·2019-09-20

    Ducati Recalls 2014-2018 Motorcycles Due to Engine Oil Leak Risk

    Ducati is recalling 651 motorcycles because engine oil may leak into the airbox and drip onto the rear tire, increasing crash risk.

    Product
    DUCATI — DUCATI 1299, 1199, PANIGALE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V667000·2019-09-19

    GM Recalls 2019-2020 Chevrolet Equinox AWD for Fuel Tank Leak Risk

    General Motors is recalling 2019-2020 Chevrolet Equinox all-wheel drive vehicles because improperly sealed fuel tank seams may leak fuel, increasing fire risk.

    Product
    CHEVROLET — CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E064000·2019-09-19

    GM Recalls Chevrolet Camaro Replacement Ignition Keys

    General Motors is recalling replacement flip-key ignition transmitters for 2010-2015 Chevrolet Camaros because the keys may accidentally turn off the engine, causing loss of power steering and braking.

    Product
    CHEVROLET — CHEVROLET CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19781·2019-09-19

    Chronicle Recalls Power Armor Helmets Due to Mold Exposure Risk

    Chronicle LLC is recalling T-51b Power Armor Collectible Helmets sold by GameStop because mold may be present on the fabric liner, posing a risk of respiratory or other infections.

    Product
    Power Armor Collectible Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19780·2019-09-19

    Exploding Kittens Recalls Safety Goggles Sold with Dodgeball Game Sets

    Exploding Kittens is recalling safety goggles sold with Extreme Edition Dodgeball game sets due to a laceration hazard from glass lenses.

    Product
    Safety Goggles sold with Throw Throw Burrito Extreme Going Pro Edition Dodgeball Card Game sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2314-2019·2019-09-18

    Teleflex Medical Recalls Sheridan Preformed Tracheal Tubes Due to Disconnection Risk

    Teleflex Medical is recalling specific lots of Hudson RCI Sheridan Preformed tracheal tubes because the 15 mm connector may disconnect from the tube, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan Preformed: a) 3.0 mm, REF 5-22006, REF 5-22106 b) 3.5 mm, REF 5-22007, REF 5-22107 c) 4.0 mm, REF 5-22008, REF 5-22108, REF 5-22208 d) 4.5 mm, REF 5-22009, REF 5-22109, REF 5-22209 e) 5.0 mm, REF 5-22010, REF 5-22110, REF 5-22210 f) 5.5 mm, REF 5-22011…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1879-2019·2019-09-18

    Plastikon Recalls Milk of Magnesia Unit Dose Cups for Microbial Contamination

    Plastikon Healthcare LLC is recalling specific lots of Milk of Magnesia unit dose cups because they failed bioburden testing for Total Aerobic Microbial Count.

    Product
    Milk of Magnesia USP, 2400 mg/30 mL, Magnesium Hydroxide 2400 mg, 30 mL unit dose cups, For Institutional Use Only, packaged in 100-count cartons of 10 trays x 10 unit dose cups, Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2452-2019·2019-09-18

    Allergan Recalls Textured Breast Implants Due to Lymphoma Risk

    Allergan is recalling 4 million textured breast implants worldwide after FDA safety updates linked them to a higher incidence of anaplastic large cell lymphoma.

    Product
    Natrelle 410, Highly Cohesive Anatomically Shaped Silicone-Filled Breast Implant Biocell Low Height Low Projection, Sterile, for the following style numbers: Syle LL: LL-410135,LL-410180,LL-410210,LL-410240,LL-410300; Style LM: LM-410140, LM-410190, LM-410220, LM-410250…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2457-2019·2019-09-18

    Allergan Natrelle Tissue Expanders Recalled for Lymphoma Risk

    Allergan is recalling Natrelle 133 tissue expanders due to FDA safety information regarding a higher incidence of anaplastic large cell lymphoma in patients with textured breast implants.

    Product
    Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable Projection with MAGNA-FINDEr Xact & 21G Needle Infusion Set STYLE 133FV-T: 133FV-11-T, 133FV-12-T, 133FV-13-T, 133FV-14-T, 133FV-15-T, 133FV-16-T; STYLE 133MV-T: 133MV-11-T, 133MV-12-T…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2460-2019·2019-09-18

    Allergan Recalls Textured Breast Implants Due to Lymphoma Risk

    Allergan is recalling specific textured breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).

    Product
    Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant, Styles LL, LM, LF, ML, MM, MF, FL, FM, FF Product Usage: Breast augmentation and Breast reconstruction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2497-2019·2019-09-18

    Aesculap Caiman Disposable Surgical Instrument Recalled for Sterility Concerns

    Aesculap Implant Systems LLC is recalling Caiman disposable articulated instruments due to a possibility that the sterility batch was insufficiently sterilized.

    Product
    CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM REF: PL731SU- Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
    Category
    Medical Device
    Distribution
    Distributed nationwide