State

Nebraska product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54776–54800 of 78407

HighFDA (Devices)·Z-0224-2016·2015-11-11
Mako RIO Robotic System Components Recalled for Damaged Locking Pins
Mako Surgical Corporation is recalling RIO system locking pins and connectors because the pins are damaged during assembly.
Product
Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated for use in surgical knee resurfacing and total hip Arthroplasty joint replacement procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0208-2016·2015-11-11
Siemens e.cam Gamma Camera Recall for Radial Brake Failure
Siemens Medical Solutions is recalling e.cam Gamma Camera systems due to a potential radial brake failure that could allow the detector to drift.
Product
e.cam Gamma Camera, an emission computed tomography system. It is intended 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 588keV.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0218-2016·2015-11-11
Brainlab Patient Data Manager Software Recalled for Image Display Errors
Brainlab AG is recalling Patient Data Manager software versions 2.0.0 through 2.1.0 because objects may display incorrectly when users deselect fused reference datasets.
Product
Digital Lightbox, BrainLAB system, image processing, radiological Product Usage: The Patient Data Manager is a system intended for the display of medical images. The software can transfer images to and from picture archiving and communication systems (PACS), file servers, or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0219-2016·2015-11-11
Philips HeartStart MRx Monitor/Defibrillator Recalled for Potential Reboot Issues
Philips is recalling HeartStart MRx monitor/defibrillators because they may reboot unexpectedly, interrupting or delaying therapy.
Product
HeartStart MRx monitor/defibrillator Models M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2016·2015-11-11
Otto Bock Triton Smart Ankle Recalled Due to Software Issue
Otto Bock is recalling the Triton Smart Ankle and iOS Galileo app due to a software issue that can cause unexpected foot movement, posing a fall risk.
Product
iOS Galileo Application Version 1.1.1 or lower that programs the Triton Smart Ankle; 1C66 Triton Smart Ankle, an external prosthetic ankle/foot.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0221-2016·2015-11-11
CareFusion Recalls SmartSite Extension Sets Due to Disconnection and Leakage
CareFusion is recalling SmartSite Extension Sets because they may disconnect or leak. The recall affects 21,000 units distributed in the US and Canada.
Product
SmartSite Extension Set, Model No. 20029E. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0226-2016·2015-11-11
GE Healthcare Recalls Centricity Universal Viewer Due to Inaccurate X-ray Measurements
GE Healthcare is recalling Centricity Universal Viewer versions 6.0 and higher because magnified projection X-ray images may display inaccurate distance measurements.
Product
The Centricity Universal Viewer Version is a device that displays medical images (including mammograms) and data from various imaging sources. Images and data can be viewed, communicated, processed and displayed within the system or across computer networks at distributed…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0225-2016·2015-11-11
GE Healthcare Recalls Centricity PACS-IW Due to Inaccurate X-Ray Measurements
GE Healthcare is recalling Centricity PACS-IW software because it may display inaccurate distance measurements for magnified projection X-ray images.
Product
The Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data from various imaging sources. Images and data can be viewed, communicated, processed and displayed within the system or across computer networks at distributed…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0204-2016·2015-11-11
Philips HeartStart MRx Monitor/Defibrillators Recalled for Capacitor Degradation
Philips is recalling 1,553 HeartStart MRx Monitor/Defibrillators because automated tests may degrade capacitors and the low battery indicator may fail.
Product
Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0163-2016·2015-11-11
Valeant Recalls Fenoglide Tablets Due to Failed Dissolution Testing
Valeant Pharmaceuticals is recalling specific bottles of Fenoglide (fenofibrate) 120 mg tablets because they failed 24-month dissolution testing.
Product
Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus, Inc. San Diego, CA 92130. NDC: 68012-495-90.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0207-2016·2015-11-11
Arrow International Recalls PICC Kits Due to Hub Tab Detachment
Arrow International Inc is recalling 12,157 units of various PICC and midline catheter kits because the peel-away component hub tabs may prematurely detach during use.
Product
ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit ARROW Advantage5 Pressure Injectable PICC Kit Arrow¿ Pressure Injectable Arrow¿ PICC powered by Arrow¿ VPS¿ Stylet ARROW Pressure Injectable JACC with Chlorag+ard Technology For short-term or…
Category
Medical Device
Distribution
36 states
ModerateFDA (Devices)·Z-0213-2016·2015-11-11
Ivoclar Recalls Helioseal F Dental Sealant Due to Production Defect
Ivoclar A. G. is recalling specific lots of Helioseal F dental sealant because a production defect caused particles to be larger than defined, resulting in difficulties during extrusion.
Product
Helioseal F Sealant Refill 1 x 1.25 g, REF 558519AN, and Helioseal F Assortment (kit) 5 x 1.25 g, REF 558518AN. Dental sealant. -- ivoclar vivadent clinical --- Helioseal F Refill is provided in a syringe packed sealed foil bag. Helioseal F is a light-curing, white-shaded…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0216-2016·2015-11-11
ELITech Clinical Systems reagents recalled for potential drug interference
ELITech Clinical Systems is recalling specific reagents used on Selectra ProS and ProM systems due to potential drug interference. No complaints have been received.
Product
ELITech Clinical Systems reagents used on the Selectra ProS and ProM systems that utilize the Trinder Reaction method. The following product reference numbers and names: GPSL-025O: Glucose PAP SL AUML-0250: URIC ACID MONO SL CHSL-0250: CHOLESTEROL SL, TGML-0250…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0231-2016·2015-11-11
Ortho-Clinical VITROS 5,1 FS Chemistry System Software Recall
Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems due to a software anomaly where user-modified parameters revert to default values during ADD installation.
Product
VITROS 5,1 FS Chemistry System, Catalog Number/Product Code 6801375, Unique Device Identifier No. 10758750001132, and VITROS 5,1 FS Chemistry System Refurbished, Catalog Number/Product Code 6801890, Unique Device Identifier No. 10758750001644. Intended for use in the in vitro…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0214-2016·2015-11-11
ELITech Eon 100 Reagents Recalled for Potential Drug Interference
ELITech Clinical Systems is recalling Eon 100 reagents due to potential drug interference. No complaints have been received.
Product
Eon 100 system included the following product reference numbers and names: Reference no. 77345- Glucose (GPSL) Reference no. 77450- Uric acid (AUVD) Reference no. 77435- Triglycerides (TGML) Reference no. 77295- Cholesterol (CHVD) Reference no. 77301- Cholesterol HDL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0227-2016·2015-11-11
Barco Surgical Display Recalled for Loss of User Settings After Power Cycle
Barco Inc. is recalling specific surgical display models because user settings are lost when the systems are powered off and back on.
Product
Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch)
Category
Medical Device
Distribution
11 states
ModerateFDA (Devices)·Z-0220-2016·2015-11-11
Dako EnVision FLEX Visualization Reagent Recalled for Staining Defect
Dako North America Inc. is recalling specific lots of EnVision FLEX visualization reagent kits due to a buffer defect causing non-specific background staining that interferes with result interpretation.
Product
EnVision FLEX/HRP visualization reagent found in the following kits: EnVision FLEX, High pH (Link) EnVision FLEX+, Mouse, High pH (Link) EnVision FLEX Mini Kit, High pH (Link) EnVision FLEX, High pH (Dako Omnis) Multi-component, sealed package. For in vitro diagnostic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0222-2016·2015-11-11
Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled
Stryker Spine is recalling 41 units of the UniVise Spinous Process Fixation Plate System Inserter because the inner shaft does not fit through the device.
Product
Stryker UniVise Spinous Process Fixation Plate System Inserter, Stryker Spine, Non-Sterile. Reference Number 48590100. Manual Surgical Instrument.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0215-2016·2015-11-11
ELITech Eon 300 Reagents Recalled for Potential Drug Interference
ELITech Clinical Systems is recalling Eon 300 reagents due to potential drug interference. No complaints have been received.
Product
Eon 300 system includes the following product reference numbers and names: Reference no. 79345 Glucose (GPSL) Reference no. 79450 Uric acid (AUVD) Reference no. 79435 Triglycerides (TGML) Reference no. 79295 Cholesterol (CHVD) Reference no. 79301 Cholesterol HDL (HDLL)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0217-2016·2015-11-11
ELITech Envoy 500 Reagent Kits Recalled for Potential Drug Interference
ELITech Clinical Systems is recalling Envoy 500 reagent kits due to potential drug interference. No complaints have been received.
Product
Envoy 500 system includes the following product reference numbers and names: 55345 ENVOY 500 Glucose 55450 ENVOY 500 URIC ACID REAGENT KIT 55435 ENVOY 500 TRIGLYCERIDES REAGENT KIT, 55297 ENVOY 500 CHOLESTEROL REAGENT KIT, 55335 ENVOY 500 CREATININE REAGENT KIT 55301…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0197-2016·2015-11-11
Philips Recalls GEMINI PET/CT Systems Due to Servo Controller Failure Risk
Philips is recalling 264 GEMINI PET/CT systems because the CT subsystem's Spindle Block Servo Controllers may fail prematurely.
Product
GEMINI PET/CT System, a diagnostic imaging system for fixed or mobile installations that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems.
Category
Medical Device
Distribution
35 states
ModerateFDA (Devices)·Z-0206-2016·2015-11-11
Bausch + Lomb Recalls Biotrue ONEday Lenses Due to Surface Defects
Bausch + Lomb is recalling Biotrue ONEday contact lenses because a manufacturing defect on the lens surface may cause visual disturbances like halos or poor vision.
Product
BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE, Rx Only; The lenses are available in 5 pack, 30 pack and 90 pack sizes; Biotrue ONEday Foil - Part Number 8098001, Biotrue ONEday 5 pack Carton International - Part Number…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0162-2016·2015-11-11
Qualitest Recalls Ranitidine Syrup Due to Preservative Stability Failure
Vintage Pharmaceuticals is recalling specific lots of Ranitidine Syrup because preservative levels failed stability specifications.
Product
RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL (75 mg/5 mL), 473 mL (16 fl oz), Rx only. Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC: 0603-9418-58.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0210-2016·2015-11-11
Steris Recalls AMSCO Steam Sterilizers Due to Foot Pedal Software Issue
Steris Corporation is recalling 32 AMSCO 400 and AMSCO C Small Steam Sterilizers because a software defect prevents the foot pedal from operating the door.
Product
AMSCO 400 and AMSCO C Small Steam Sterilizers
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0202-2016·2015-11-11
Ortho-Clinical VITROS Calibrator Kit 9 Recall for Wash Errors
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 9, Lot 0954, due to an increase in wash error condition codes.
Product
VITROS Chemistry Products Calibrator Kit 9 Calibrator, 2 mL, Product Code 8568040, Unique Device Identifier No. 10758750005031, IVD -- Ortho Clinical Diagnostics, Inc. --- VITROS Chemistry Products Calibrator Kit 9 is used to calibrate VITROS 250/350/950/5,1 FS and 4600…
Category
Medical Device
Distribution
Distributed nationwide