State

Nevada product recalls

73,363 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total: 5,696
Critical: 951
Severe: 1,479
Most recent: 2026-09-25

Of the 5,696 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,479 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17226–17250 of 79059

HighFDA (Devices)·Z-1505-2023·2023-05-10
Siemens ADVIA Centaur Cortisol Diagnostic Kits Recalled for Negative Measurement Bias
Siemens Healthcare Diagnostics is recalling 18,961 ADVIA Centaur Cortisol diagnostic kits due to negative bias in urine samples causing intermittently low test results that could affect clinical diagnosis.
Product
ADVIA Centaur Cortisol 50T (Material Number 10994924), ADVIA Centaur Cortisol 250T (Material Number 10994926), and ADVIA Centaur Cortisol REF 250T (Material Number 10994927). In vitro diagnostic use in the quantitative determination of cortisol in human serum, plasma (EDTA and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2023·2023-05-10
Angiography System C-Arm Positioning Malfunction May Cause Patient Injury
Siemens ARTIS pheno angiography systems may misposition the C-arm by 5-10 millimeters when using the reference image positioning function, risking patient and staff crushing injuries. The device may also display inaccurate imaging overlays, potentially causing vessel perforation.
Product
ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET table (OEM)- Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Model: 10849000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1503-2023·2023-05-10
FDA Class II Recall: Ultraview SL Command Module Monitoring Alarms May Fail
Spacelabs Healthcare is recalling 1,088 Ultraview SL Command Module units due to a software defect. The devices may fail to display alarms or waveforms when parameter processing is suspended, potentially causing clinicians to miss critical patient events.
Product
Ultraview SL (UVSL) Command Module, Model 91496
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1550-2023·2023-05-10
LINK SLED Knee Implant Recall for Aseptic Loosening Risk
The LINK SLED Knee System POREX ENDO tibial implant is recalled due to risk of early aseptic loosening or increased wear from suboptimal positioning or inadequate cementing. Affected patients may require early revision surgery.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 11 MM X 55 MM Item Number: 15-2230/11
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0788-2023·2023-05-10
Soy Flour Recalled for Undeclared Gluten in Gluten-Free Products
Cargill is recalling PROSANTE TSOYFLR flour products labeled gluten-free because they may contain gluten above 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume these products.
Product
PROSANTE TSOYFLR 3P MNCD 50LB BG, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2023·2023-05-10
Knee implant component recalled for risk of premature loosening and wear
Linkbio Corp. is recalling 14 units of LINK SLED Knee System knee implant components due to risk of early loosening and wear caused by suboptimal implant positioning or inadequate cementing technique. Affected patients should contact their surgeon.
Product
LINK SLED Knee System: ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2020/40
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0783-2023·2023-05-10
Cargill Flour Recalled Due to Undeclared Gluten Contamination
Cargill is recalling PROSANTE TSOYFLR flour products nationwide and internationally due to potential gluten contamination in products labeled as gluten-free. The recalled products may contain gluten levels above 20 ppm.
Product
PROSANTE TSOYFLR 3014P FLK 50LB BG, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0797-2023·2023-05-10
Cargill recalls PROSANTE product with undeclared gluten in gluten-free labeling
Cargill is recalling PROSANTE TVGPTN 5B product because items labeled gluten-free may contain gluten above 20 ppm. The recall affects 496,200 lbs distributed nationwide and internationally.
Product
PROSANTE TVGPTN 5B MNCD 50LB BG, PROSANTE TVGPTN 5B MNCD 50LB BG/21P, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0785-2023·2023-05-10
Cargill Prosante gluten-free products may contain excessive gluten levels
Cargill's Prosante products labeled gluten-free may contain gluten exceeding 20 ppm. The recall affects 4.6 million pounds distributed in the United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and the United Kingdom.
Product
PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROSANTE TVGPTN 10B MNCD 50LB BG, PROSANTE TVGPTN 10B MNCD 50LB BG 21/P; distributed in bulk tote and paper bags
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1520-2023·2023-05-10
LINK SLED Knee Implant Component Recalled for Early Aseptic Loosening Risk
Linkbio Corp. is recalling 13 units of the LINK SLED Knee Implant All Poly Tibial Component due to risk of early aseptic loosening from suboptimal surgical positioning or inadequate cementing technique. Updated surgical technique guidance is being provided to prevent premature implant failure.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 9MM X 55MM Item Number: 15-2028/10
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0794-2023·2023-05-10
Gluten-Free Labeled Food Product May Contain Undeclared Gluten
Cargill is recalling PROSANTE products labeled as gluten-free that may contain gluten above safe levels (above 20 ppm). Consumers following a gluten-free diet should discontinue use of affected products.
Product
PROSANTE TVGPTN 10BF7 MNCD 50LB BG/36P, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1543-2023·2023-05-10
LINK SLED Knee System Tibial Component Recall Due to Surgical Technique Issues
Linkbio Corp. is recalling LINK SLED Knee System tibial components due to risk of early aseptic loosening or premature wear caused by suboptimal implant positioning or inadequate cementing during surgery. The manufacturer is updating surgical technique guidance and training.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 45 MM Item Number: 15-2230/02
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1547-2023·2023-05-10
Knee implant system recalled due to aseptic loosening and wear risk
Linkbio Corp. is recalling the LINK SLED Knee System due to risk of early aseptic loosening and increased wear caused by improper surgical technique or positioning. The issue may require early revision surgery.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 11 MM X 50 MM Item Number: 15-2230/07
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0790-2023·2023-05-10
Cargill Vegetable Protein Recalled for Undeclared Gluten Content
Cargill is recalling PROSANTE vegetable protein bags labeled as gluten-free because they may contain gluten levels exceeding 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume the affected product.
Product
PROSANTE TVGPTN 5PF MNCD 50LB BG, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1561-2023·2023-05-10
Laboratory Automation System Firmware May Misidentify Patient Samples
Inpeco laboratory automation systems' firmware can misassociate patient samples, potentially leading to incorrect electrolyte test results. The defect is rare but could cause serious medical consequences if results are misidentified or delayed.
Product
PVT Interface Module (PVT)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: 72747000.A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1519-2023·2023-05-10
LINK SLED Knee System Tibial Component Recall Due to Early Loosening Risk
Linkbio Corp. is recalling the LINK SLED Knee System ALL POLY TIBIAL COMPONENT due to risk of early aseptic loosening or increased wear from suboptimal surgical placement or cementing, which may require early revision surgery.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 55MM Item Number: 15-2028/09
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1544-2023·2023-05-10
Knee Implant Component Recalled for Surgical Positioning and Cementing Guidance
FDA is updating surgical instructions for the LINK SLED Knee System to address early aseptic loosening and increased wear from suboptimal positioning or inadequate cementing technique. Updated training aims to prevent implant failure and unexpected revision surgery.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 11 MM X 45 MM Item Number: 15-2230/03
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1527-2023·2023-05-10
LINK SLED Knee System Tibial Component Recall for Aseptic Loosening Risk
Linkbio Corp. is recalling the LINK SLED Knee System tibial component due to risk of aseptic loosening and wear. The recall addresses concerns about suboptimal implant positioning or inadequate cementing technique that could lead to early revision surgery.
Product
LINK SLED Knee System: ENDO MODEL SLED TIBIAL COMP 9 MM X 45 MM Item Number: 15-2030/02
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1516-2023·2023-05-10
LINK SLED Knee System tibial component subject to surgical technique amendment
A knee implant component is being recalled due to risks of early loosening or increased wear caused by suboptimal implant positioning or inadequate cementing. Manufacturers are providing updated surgical guidance.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 9MM X 50MM Item Number: 15-2028/06
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1542-2023·2023-05-10
Knee Implant System Recalled for Risk of Aseptic Loosening
Linkbio Corp. recalls the LINK SLED Knee System due to risk of aseptic loosening from improper positioning or cementing technique, potentially requiring revision surgery. Five units affected in US and international distribution.
Product
LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, LARGE Item Number: 15-2220/60
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1541-2023·2023-05-10
LINK SLED Knee System implants recalled for early loosening risk
Linkbio Corp. recalls 7 LINK SLED knee implants due to risk of early aseptic loosening and increased wear caused by suboptimal surgical technique. Affected units may require earlier-than-expected revision surgery.
Product
LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, MEDIUM Item Number: 15-2220/52
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1549-2023·2023-05-10
LINK SLED Knee System recalls due to implant loosening risk
Linkbio Corp. is recalling LINK SLED Knee System implants that may loosen prematurely due to improper positioning or cementing technique. Enhanced surgical training is being provided to prevent early device failure.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 55 MM Item Number: 15-2230/10
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1539-2023·2023-05-10
Orthopedic knee implant system recalled due to early loosening risk
Linkbio Corp. is recalling 5 units of the LINK SLED Knee System due to risk of early aseptic loosening or increased wear that could require earlier surgical revision. The recall addresses training and surgical technique to prevent implant failure.
Product
LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2220/40
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0801-2023·2023-05-10
Cargill Grain Product Recalled for Gluten Contamination Despite Gluten-Free Label
Cargill is recalling PROSANTE TVGPTN products labeled as gluten-free because they may contain gluten levels above 20 ppm. The recall affects 42,400 pounds distributed nationwide and internationally.
Product
PROSANTE TVGPTN 10P MNCD 25LB BG/32P, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1533-2023·2023-05-10
LINK SLED Knee System Recalled for Aseptic Loosening and Implant Wear
Linkbio Corp. is recalling 12 units of the LINK SLED Knee System due to risk of implant loosening and wear that could require revision surgery sooner than expected.
Product
LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 9 MM X 55 MM Item Number: 15-2030/10
Category
Medical Device
Distribution
2 states