The Recall Desk

State

Nebraska product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36101–36125 of 78318

  • ModerateFDA (Devices)·Z-1407-2019·2019-05-29

    Remel Thio Med w/Dex, Hem, Vit K Media Recall for Performance Failure

    Remel Inc is recalling Thio Med w/Dex, Hem, Vit K media because it may fail performance testing after 106 days. The expiration date is being shortened to 105 days.

    Product
    Thio Med w/Dex, Hem, Vit K(10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1477-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.

    Product
    Drill, cannulated, 2.5x95mm, round shaft, Item Number ST502015620
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1443-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications. The products were distributed to 41 US states.

    Product
    Drill, cannulated, 3x90mm, round shaft, Item Number 502015630
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1451-2019·2019-05-29

    Zimmer GmbH Recalls AO Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling specific AO orthopedic drills because they may be made from the wrong material. The products were distributed to 39 US states.

    Product
    Drill, 3.2x145mm, AO, Item Number 502015650
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1432-2019·2019-05-29

    Zimmer GmbH Recalls 3.5mm Screw Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 3.5mm screw drills because they may be made from a different material than specified.

    Product
    Drill for 3.5mm screw, 2.5x120mm, AO, Item Number 502015216
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1400-2019·2019-05-29

    Remel Thio Med Culture Media Recalled for Potential Performance Failure

    Remel Inc is recalling Thio Med culture media because the product may fail performance testing after 106 days. The expiration date is being shortened from 9 months to 105 days.

    Product
    Thio Med w/o Ind, w/Dex (9ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1369-2019·2019-05-29

    Cook Kwart Retro-Inject Ureteral Stent Set Recalled for Missing Warning

    Cook Inc. is recalling Kwart Retro-Inject Ureteral Stent Sets because the instructions for use did not include a warning for stent knotting.

    Product
    Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7 Fr 003500 G14916; 6.0 Fr 003600 G14836; 7.0 Fr 003700 G14837; 8.0 Fr 003800 G14844; Set with AQ¿ Hydrophilic Coating PRODUCT/CATALOG NUMBER/GPN: 4.7 Fr AQ-003500 G17150; 6.0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1484-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Concerns

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications.

    Product
    Drill, cannulated, 4x90mm, round shaft, Item Number ST502015640
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1429-2019·2019-05-29

    Stryker 2.7mm Screw Drill Recalled for Material Specification Deviation

    Zimmer GmbH is recalling Stryker 2.7mm screw drills because they may have been manufactured from a material different from the specifications.

    Product
    Drill for 2.7mm screw, 2x125mm, Stryker, Item Number 502015211
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1487-2019·2019-05-29

    Zimmer GmbH Recalls CBS Micro Countersink Cannulated AO Screws

    Zimmer GmbH is recalling CBS micro, countersink, cannulated, AO screws (Item Number ST503004541) because they may have been manufactured from a different material than specified.

    Product
    CBS micro, countersink, cannulated, AO, Item Number ST503004541
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Drugs)·D-1307-2019·2019-05-29

    Septodont Recalls Articadent Dental Cartridges Due to Carton Mislabeling

    Septodont Inc. is recalling 240 cartons of Articadent dental cartridges because the printed cartons contained text for both Articadent and Xylocaine, though the cartridges themselves are correctly labeled.

    Product
    ARTICADENT — ARTICADENT (ARTICAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1405-2019·2019-05-29

    Remel Thio Med Media Recalled for Potential Performance Failure

    Remel Inc is recalling Thio Med w/o Ind, w/Dex media because it may fail performance testing after 106 days. The expiration date is shortened from 9 months to 105 days.

    Product
    Thio Med w/o Ind, w/Dex (10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1409-2019·2019-05-29

    Remel Thio Med w/o Ind, w/Dex Recalled for Potential Performance Failure

    Remel Inc is recalling 27 units of Thio Med w/o Ind, w/Dex due to potential failure in performance testing after 106 days.

    Product
    Thio Med w/o Ind, w/Dex (18ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1426-2019·2019-05-29

    Stryker 2.7mm Screw Drill Recalled for Material Specification Deviation

    Zimmer GmbH is recalling Stryker 2.7mm screw drills because they may be made from a different material than specified.

    Product
    Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number 502015206
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1467-2019·2019-05-29

    Zimmer GmbH Recalls V-TEK Micro-countersink Due to Material Concerns

    Zimmer GmbH is recalling V-TEK Micro-countersink items because they may be made from the wrong material. The products were distributed to 39 US states.

    Product
    V-TEK", Micro-countersink, AO , Item Number ST28.66.113
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1442-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.

    Product
    Drill, cannulated, 2.8x150mm, AO, Item Number 502015629
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1390-2019·2019-05-29

    Thommen Medical Recalls Dental Adapters for Handpiece Due to Deformation Risk

    Thommen Medical AG is recalling 15 units of dental adapters for handpieces because the coupling may deform, making removal difficult.

    Product
    Adapter for handpiece, guided, reusable, for guide sleeve 0 4.8 mm Article number: 3.04.090 - Product Usage: The adapter for handpiece, guided reusable, for guide sleeve ¿ 4.8 mm is used to transfer the implant from the packaging to the patient via a plug-in connection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1444-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than defined in specifications.

    Product
    Drill, cannulated, 3x90mm, AO, Item Number 502015631
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1452-2019·2019-05-29

    Zimmer GmbH Recalls Contra-Angle Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling contra-angle drills that may have been manufactured from a different material than specified. The products were distributed to 41 US states.

    Product
    Drill, contra-angle, 1.5x85mm, Item Number 502015706
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1378-2019·2019-05-29

    Remel Inc Recalls Thio Med w/Dex, Hemin, Vit K Media

    Remel Inc is recalling Thio Med w/Dex, Hemin, Vit K media because the products may fail performance testing after 57 days.

    Product
    Thio Med w/Dex, Hemin, Vit K (5ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1482-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

    Zimmer GmbH is recalling specific cannulated drills that may have been manufactured from a material different from the defined specifications.

    Product
    Drill, cannulated, 3x90mm, AO, Item Number ST502015631
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1417-2019·2019-05-29

    Stryker 26mm Drill Recalled for Potential Material Specification Deviation

    Zimmer GmbH is recalling Stryker 26mm drills because an investigation found they may have been manufactured from a different material than specified.

    Product
    Drill, 26mm stop, 1.4x94mm, Stryker, Item Number 502015120
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-1402-2019·2019-05-29

    Remel Thio Med Culture Media Recalled for Potential Performance Failure

    Remel Inc is recalling Thio Med culture media due to potential failure to meet performance standards after 106 days from manufacturing.

    Product
    Thio Med w/o Ind, w/Dex (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes
    Category
    Medical Device
    Distribution
    Distributed nationwide