The Recall Desk

State

Nebraska product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42076–42100 of 78386

  • HighFDA (Devices)·Z-0896-2018·2018-03-14

    Medtronic Recalls Unimplanted SynchroMed II Pumps Due to Motor Stall Risk

    Medtronic is recalling unimplanted SynchroMed II Model 8637 pumps to address a design flaw that can cause motor stalls due to corrosion.

    Product
    Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The implantable Model 8637 SynchroMed II programmable pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implanted…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0850-2018·2018-03-14

    Philips Network Firewall Recall Due to Defective Clock Component

    Philips is recalling 332 network firewalls used with IntelliVue systems due to a defective clock component that may cause loss of connection.

    Product
    Philips Network Firewall (Cisco ASA 5506), Model # 867098
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2018·2018-03-14

    DePuy Concorde Lift Driver Shaft Recalled for Potential Breakage

    DePuy Orthopaedics is recalling 130 units of the Concorde Lift Driver Shaft AO due to a potential for intra-operative breakage of driver tips.

    Product
    Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0898-2018·2018-03-14

    Heartland Coca-Cola Recalls Orange Fanta Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Orange Fanta cans because sharp edges on the cans could cause cuts to consumers' mouths.

    Product
    Orange Fanta, Orange soda, Naturally flavored, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0892-2018·2018-03-14

    Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blade Complaints

    Bausch & Lomb Inc Irb is voluntarily recalling LASEREDGE Knives intended for ophthalmic surgery because of an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, 2.0MMX2.2MM TRAPEZOID ANGLED GUARDED (6/BOX), REF/PRODUCT CODE E7601G, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0904-2018·2018-03-14

    Fresca Citrus Soda Recalled Due to Sharp Can Edges

    Heartland Coca-Cola Bottling Company is recalling Fresca Original Citrus Sparkling Flavored Soda cans because sharp edges were observed that could cause cuts to consumers' mouths.

    Product
    Fresca, Original Citrus Sparkling Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0905-2018·2018-03-14

    Heartland Coca-Cola Recalls Strawberry Fanta Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Strawberry Fanta cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Strawberry Fanta, Strawberry Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0910-2018·2018-03-14

    Roche cobas 8000 Modular Analyzer Recall for Operator Injury Prevention

    Roche Diagnostics is recalling 245 cobas 8000 c 502 modules to add a warning to the manual, preventing operator injury during maintenance.

    Product
    cobas 8000 Modular Analyzer Series; Part Numbers: 1. 05964067001 cobas 8000 c 502 module
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Food)·F-0900-2018·2018-03-14

    Coca-Cola Zero Sugar Cans Recalled for Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling specific lots of Coca-Cola Zero Sugar cans due to sharp edges that could cause mouth cuts.

    Product
    Coca-Cola, Zero Sugar, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0907-2018·2018-03-14

    Dr Pepper Cans Recalled Due to Sharp Edges Causing Potential Cuts

    Heartland Coca-Cola Bottling Company is recalling Dr Pepper 12 oz cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Dr Pepper, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of Dr Pepper Company, Plano, TX
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0896-2018·2018-03-14

    Heartland Coca-Cola Recalls Caffeine Free Coke Zero Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Caffeine Free Coke Zero cans because sharp edges were observed that could cause cuts to consumers' mouths.

    Product
    Caffeine Free Coke Zero, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0901-2018·2018-03-14

    Synthes Reaming Rods Recalled for Potential Sterility Seal Defects

    Synthes (USA) Products LLC is recalling 2.5 mm Reaming Rods because package seal defects may have compromised sterility. The devices are used in orthopedic surgery.

    Product
    2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers during orthopedic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0888-2018·2018-03-14

    Heartland Coca-Cola Recalls Pibb Xtra Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Pibb Xtra soda cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Pibb Xtra, Artificially Flavored Spicy Cherry Soda 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0901-2018·2018-03-14

    Coca-Cola Vanilla Cans Recalled for Sharp Edges Causing Mouth Cuts

    Heartland Coca-Cola Bottling Company is recalling 766,271 cases of 12 oz Vanilla Coca-Cola cans due to sharp edges that may cause cuts.

    Product
    Coca-Cola, Vanilla Flavor, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0895-2018·2018-03-14

    Heartland Coca-Cola Recalls Diet Coke Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Diet Coke Caffeine Free cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Diet Coke Caffeine Free, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighCPSC·18123·2018-03-14

    Cameron Company Recalls Children's Tents Due to Laceration Hazard

    Cameron Company is recalling Playtime Pals Pop-Up Hideaway Hut children's tents because the fiberglass support rods can break and splinter, posing a laceration hazard.

    Product
    Playtime Pals Pop-Up Hideaway Hut children's tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0897-2018·2018-03-14

    Heartland Coca-Cola Recalls Diet Coke Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling 766,271 cases of Diet Coke cans because sharp edges were observed, posing a risk of mouth cuts.

    Product
    Diet Coke, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0920-2018·2018-03-14

    Signature Ceramic Femoral Head Recalled for Mislabeled Packaging

    Signature Orthopedics is recalling 10 ceramic femoral heads because the packaging labels do not match the component sizes, which may cause surgical delays.

    Product
    Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature ceramic femoral heads are manufactured by Ceramtec from 72-75% Al2O3+24-26% Z3O3 (Biolox Delta). The heads connect via a 12/14 taper to the stem trunnion, and articulates against the crosslinked UHMWPE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0940-2018·2018-03-14

    Springside Monterey Jack Cheese Recalled Due to Pasteurization Error

    Springside Cheese Corp is recalling 129.4 lbs of Monterey Jack Garden Vegetable Cheese because the milk may not have been pasteurized long enough.

    Product
    Springside Monterey Jack Garden Vegetable Cheese, 40 lbs.
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Drugs)·D-0914-2018·2018-03-14

    Ranitidine Tablets Recalled for Failed Stability Specifications

    Mckesson Packaging Services is recalling Ranitidine Tablets 150 mg due to failed stability specifications. The recall affects 17,192 cartons distributed nationwide.

    Product
    RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0855-2018·2018-03-14

    Bausch + Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch + Lomb is voluntarily recalling 1,236,749 LaserEdge ophthalmic knives due to an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, CRESCENT KNIFE BEVELED UP ANGLED (6/BOX), REF/PRODUCT CODE E7510G, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0883-2018·2018-03-14

    Bausch + Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch + Lomb is voluntarily recalling 1,236,749 LaserEdge ophthalmic knives because of an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, KNIFE ANGLED BEVELED UP 2.7(6/BOX), REF/PRODUCT CODE E7559A, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0942-2018·2018-03-14

    Springside Monterey Jack Jalapeno Cheese Recalled for Pasteurization Issue

    Springside Cheese Corp is recalling Monterey Jack Jalapeno Cheese because it may have been made with milk held for 13.8 seconds during pasteurization.

    Product
    Springside Monterey Jack Jalapeno Cheese packaged in the following sizes: Net Wt. 8 oz., 1 lb. and 40 lbs.
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0912-2018·2018-03-14

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products DAT Performance Verifier II

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products DAT Performance Verifier II because storage labeling errors may cause lower than expected VITROS BENZ results.

    Product
    VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide