State

Nebraska product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47101–47125 of 78397

HighFDA (Drugs)·D-0544-2017·2017-03-22
Synergy Rx Recalls Trichloroacetic Acid Solutions Due to Sterility Concerns
Synergy Rx is recalling Trichloroacetic Acid Solutions in various strengths due to a lack of assurance of sterility and CGMP deviations.
Product
TRICHLOROACETIC ACID SOLUTION in all strengths including: 10%, 12%, 15 %, 20%, 35%, 70%, and 85%, TRICHLOROCETIC ACID 10%/ LACTIC ACID 12%, TRICHLOROCETIC ACID 6%/LACTIC ACID 12%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0586-2017·2017-03-22
Synergy Rx Recalls Hydroquinone Cream Due to Sterility Assurance Concerns
Synergy Rx is recalling Hydroquinone Cream in all strengths due to a lack of assurance of sterility and CGMP deviations.
Product
HYDROQUINONE CREAM in all strengths including: 4%, 5%, 6%, 7%, 8%,10%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0529-2017·2017-03-22
Synergy Rx Recalls Bicarbonate 10% Due to Sterility Assurance Concerns
Synergy Rx is recalling Bicarbonate 10% because the product lacks assurance of sterility and has CGMP deviations.
Product
BICARBONATE 10%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0575-2017·2017-03-22
Synergy Rx Recalls TRI-BLEACHING CREAM Due to Sterility Assurance Issues
Synergy Rx is recalling TRI-BLEACHING CREAM because it lacks assurance of sterility and has CGMP deviations. The product is distributed nationwide.
Product
TRI-BLEACHING CREAM (Retinoic Acid 0.1%, Hydroquinone 4%, Fluocinolone 0.01%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2017·2017-03-22
CareFusion Recalls MaxGuard Extension Sets Due to Filter Leaks
CareFusion is recalling 12,850 MaxGuard Extension Sets because the 0.2 micron filter may leak. These medical devices are used to administer fluids to patients.
Product
MaxGuard Extension Set, Model No. ME2064, MP9009C, MP9209, MP9254C The MaxGuard extension sets are used to administer fluids from a container to a patient s vascular system through a needle or catheter inserted into the patient s artery or vein. The extension sets may…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1481-2017·2017-03-22
Philips BrightView X Nuclear Imaging System Recalled for Four Software and Hardware Issues
Philips Medical Systems is recalling 1,218 BrightView X nuclear imaging systems worldwide due to four issues: motion controller failures, door interlock problems, detector contact risks, and software freezes.
Product
882478: BrightView X designed for single or dual detector nuclear imaging accommodating a range of ECT studies. In addition it can be used to perform planar static, dynamic, gated, total body, circular-orbit and noncircular orbit SPECT, gated SPECT (circular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2017·2017-03-22
C2 CryoBalloon Controller Cap Recall Due to Cracking Risk
C2 Therapeutics is recalling 755 C2 CryoBalloon Controller Caps because they may crack when tightened, potentially compromising the device's integrity.
Product
C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller; Cryosurgical Unit, Cryogenic Surgical Device The affected product is the Controller Cap component only, which is provided to the customer already assembled onto the Controller. Model number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1442-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Labeling
LeMaitre Vascular is recalling Reddick Cholangiogram Catheters because the latex symbol was not printed on the packaging, posing a risk to latex-allergic patients.
Product
LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1452-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Labeling
LeMaitre Vascular is recalling 2,065 units of Scoop Tip Cholangiogram Catheters because the latex symbol was not printed on the packaging.
Product
LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-53
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·029-2017·2017-03-22
Whiskey Hill Smokehouse Recalls Jerky for Undeclared Soy Allergen
Whiskey Hill Smokehouse is recalling beef, venison, and ostrich jerky because the products contain soy, a known allergen, that is not declared on the label.
Product
Whiskey Hill Smokehouse LLC — Whiskey Hill Smokehouse LLC. Recalls Beef, Venison and Ostrich Jerky Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0566-2017·2017-03-22
Synergy Rx Modified Jessner Peel Recalled for Sterility Assurance Issues
Synergy Rx is recalling Modified Jessner Peel due to lack of assurance of sterility and CGMP deviations.
Product
MODIFIED JESSNER PEEL (Sal Acid 14%, Lactic Acid 14%, glycolic 14%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0543-2017·2017-03-22
Synergy Rx Recalls Salicylic Acid and 5-FU Products for Sterility Concerns
Synergy Rx is recalling salicylic acid and 5-FU prescription products due to lack of assurance of sterility and CGMP deviations.
Product
SALICYLIC ACID SOLUTION in all strengths including 20%, 25%, 30%, and 40%, SALICYCLIC ACID 20%. 2.5%5-FU, SALICYCLIC ACID 20%, 5-FU 2.5% CREAM, SALICYCLIC ACID 20%/5-FU 2.5% MEDICATION STICK, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2017·2017-03-22
LeMaitre Vascular Catheter Recalled for Missing Latex Warning Symbol
LeMaitre Vascular is recalling Reddick Scoop Tip Cholangiogram Stiffer Catheters because the latex warning symbol was missing from the packaging.
Product
LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper IFU) REF# 2401-50
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1461-2017·2017-03-22
Kiscomedica Recalls L-Varlock Cage/Trial Implant Holder Due to Breakage
Kiscomedica S.A. is recalling 13 units of the L-Varlock Cage/Trial Implant Holder because the tip holder broke during use.
Product
L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0588-2017·2017-03-22
Synergy Rx Recalls Tretinoin Cream and Gel Due to Sterility Concerns
Synergy Rx is recalling Tretinoin Cream and Gel in all strengths due to a lack of assurance of sterility and CGMP deviations.
Product
TRETINOIN CREAM in all strengths including: 0.1%, 0.05%, TRETINOIN GEL in all strengths including 0.1% and 0.05%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1397-2017·2017-03-22
Toshiba Kalare X-ray Generator Recalled for Premature Exposure Termination
Toshiba American Medical Systems Inc is recalling 254 Kalare DREX-KL80 X-ray generators because the system may terminate exposure prematurely during an examination.
Product
Toshiba Kalare DREX-KL80 X-ray generator
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1480-2017·2017-03-22
Philips BrightView Nuclear Imaging Systems Recalled for Motion and Software Issues
Philips Medical Systems is recalling 1,218 BrightView nuclear imaging systems worldwide due to four issues, including motion controller failures and software freezes.
Product
882480: BrightView designed for single or dual detector nuclear imaging accommodating a range of ECT studies. In addition it can be used to perform planar static, dynamic, gated, total body, circular-orbit and noncircular orbit SPECT, gated SPECT (circular and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1465-2017·2017-03-22
Smiths Medical Recalls Mislabelled Pediatric Tracheostomy Tubes
Smiths Medical is recalling 142 Bivona TTS Pediatric Tracheostomy Tubes because they were incorrectly labeled for neonatal use instead of pediatric use.
Product
Bivona¿ TTS (Tight to Shaft) Pediatric Tracheostomy Tube, Model No. 67SP035, Reorder No. 67SP035.
Category
Medical Device
Distribution
20 states
ModerateFDA (Devices)·Z-1444-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Symbol
LeMaitre Vascular is recalling 608 Reddick Cholangiogram Catheters because the latex warning symbol was not printed on the packaging.
Product
LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF # e2400-52
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1466-2017·2017-03-22
Siemens Artis Q and Q.Zen Fluoroscopic X-Ray System Recall
Siemens is recalling Artis Q and Q.Zen fluoroscopic x-ray systems because a gap in the wireless foot switch housing could allow liquids to penetrate the interior, potentially causing the switch to fail.
Product
Artis Q and Q.Zen fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1451-2017·2017-03-22
LeMaitre Vascular Cholangiogram Catheter Recalled for Missing Latex Symbol
LeMaitre Vascular is recalling 247 units of Scoop Tip Cholangiogram Catheters because the latex warning symbol was missing from the packaging.
Product
LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper IFU) REF# 2401-52
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1458-2017·2017-03-22
Terumo Level Sensor II Pads Recalled for Non-Compliant Expiration Date Labeling
Terumo Cardiovascular Systems Corporation is voluntarily recalling Level Sensor II Pads because the expiration date format may not be recognizable to all users.
Product
Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the transmission of sound energy between the level sensor and the reservoir.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0542-2017·2017-03-22
Synergy Rx Recalls Retinoic Acid Solution Due to Sterility Concerns
Synergy Rx is recalling all lots of Retinoic Acid Solution due to a lack of assurance of sterility and CGMP deviations.
Product
RETINOIC ACID SOLUTION in all strengths including 0.3%, 0.4%, 0.5%, 1%, RETINOIC ACID SOLUTION LIQUID, 0.4%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0592-2017·2017-03-22
Synergy Rx Recalls RETIN-A 0.05% Cream Due to Sterility Concerns
Synergy Rx is recalling RETIN-A 0.05% Cream because of a lack of assurance of sterility and CGMP deviations.
Product
RETIN-A 0.05% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1459-2017·2017-03-22
Terumo Level Sensor Gel Pads Recalled for Non-Compliant Labeling
Terumo is voluntarily recalling Level Sensor II Gel Pads because the expiration date format may not be recognizable to all users.
Product
Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Usage: Level sensor pads are used to attach the level sensors to a hard shell reservoir. includes coupling gel.
Category
Medical Device
Distribution
Distributed nationwide