State

Utah product recalls

73,737 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,914
Critical: 524
Severe: 1,350
Most recent: 2026-10-28

Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28326–28350 of 78651

HighFDA (Devices)·Z-0625-2021·2020-12-23
Biomet Phoenix Interlocking Screws Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of Phoenix interlocking screws because a breach in the sterile seal could lead to loss of sterility.
Product
PHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14-405070 - Product Usage: Fracture fixation of small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0626-2021·2020-12-23
Biomet RapidFire Clip Recall Due to Potential Sterile Seal Breach
Biomet is recalling specific lots of RapidFire Clips used for craniofacial bone fixation because a breach in the sterile seal could lead to loss of sterility.
Product
RapidFire Clip, Item Number 95-0154 - Product Usage: Fixation of Craniofacial bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0631-2021·2020-12-23
Biomet RingLoc+ Drill Bits Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of RingLoc+ Quick Connect Drill Bits because a breach in the sterile seal could lead to loss of sterility.
Product
RingLoc+ Quick Connect Drill Bit, Item numbers 31-323215, 31-323220, 31-323230, 31-323240 - Product Usage: Bit, Drill.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0616-2021·2020-12-23
Biomet Recalls Cannulated Screw Systems Due to Potential Sterile Seal Breach
Biomet is recalling specific lots of cannulated screw systems because a breach in the sterile seal could lead to loss of sterility.
Product
3.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009787 110009790, 110009794, 110009796, 110009798, 110009800 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0624-2021·2020-12-23
Biomet Oxford Fixed Lateral Knee Implants Recalled for Sterile Seal Breach
Biomet is recalling specific lots of Oxford Fixed Lateral knee implants because a breach in the sterile seal could lead to loss of sterility.
Product
Oxford Fixed Lateral, Item numbers 154330, 154370, 154373 154376 - Product Usage: indicated for use in the lateral compartment and intended to be implanted with bone cement.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0564-2021·2020-12-23
FDA Recalls Tempus LS Manual Defibrillators Due to Software Error
Remote Diagnostic Technologies is recalling 175 Tempus LS manual defibrillators because a software error may delay therapy by disrupting ECG calibration.
Product
Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in the following environmental: - Primarily in pre-hospital care and transport applications (including ambulances, fixed and rotary wing aircraft).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0590-2021·2020-12-23
Enterix Recalls InSure ONE Test Strips Due to Potential False Positives
Enterix, Inc. is recalling InSure ONE Test Strips because they may produce false positive results, potentially leading to unnecessary medical procedures.
Product
InSure ONE Test Strips (25 pack) vials-fecal immunochemical test (FIT) qualitatively detects human hemoglobin from blood in fecal samples Model 12045.01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0589-2021·2020-12-23
RaySearch Recalls RayStation and RayPlan Software Due to Treatment Plan Errors
RaySearch is recalling RayStation and RayPlan software versions due to potential errors in treatment plan reports, including incorrect dose information and couch angles.
Product
RayStation 4, 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, RayPlan 1, 2, 7, 8A, 8B, 9A, 9B, including all service packs. RayStation 10A and RayPlan 10A are also affected, but not the 10A service pack. (Model No. 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0, 9.1…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21057·2020-12-23
GSK Recalls Five Excedrin Brands Due to Child-Resistant Packaging Defects
GSK Consumer Healthcare is recalling five Excedrin brands because some bottles have holes in the bottom, posing a risk of poisoning to children.
Product
Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0623-2021·2020-12-23
Biomet OSS Polyethylene Tibial Bushing Recalled for Sterile Seal Breach
Biomet is recalling specific lots of OSS Polyethylene Tibial Bushings because a breach in the sterile seal could lead to loss of sterility.
Product
OSS Polyethylene Tibial Bushing, Item number 150476 - Product Usage: intended for use in limb salvage.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0613-2021·2020-12-23
Carl Zeiss Meditec VISULENS 550 Recalled for Electrical Shock Risk
Carl Zeiss Meditec is recalling VISULENS 550 refractive power measurement devices due to a defective communication board that may cause electrical shocks.
Product
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of contact lenses and spectacle lenses and displaying measurement values for sphere, cylinder and prism.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0629-2021·2020-12-23
Biomet Recalls Sterile Trac System Thinflap Burr Hole Plates
Biomet is recalling specific lots of Sterile Trac System Thinflap 24 MM Burr Hole Plates because a breach in the sterile seal could lead to loss of sterility.
Product
Sterile Trac System Thinflap 24 MM Burr Hole Plate, Item number SP-STA-1021-12 - Product Usage: Fixation of Cranial bone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0620-2021·2020-12-23
Biomet Shoulder System Surgical Handles Recalled for Sterile Seal Breach
Biomet is recalling specific lots of sterile shoulder system surgical instrument handles because a breach in the packaging seal could lead to loss of sterility.
Product
Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System, Item number 406669 - Product Usage: Surgical instrument handle, non-torque-limiting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0621-2021·2020-12-23
Biomet Custom Cancellous Thread Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of Custom Cancellous Thread devices because a breach in the sterile seal could lead to loss of sterility.
Product
Custom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1. Noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis 3. Correction of functional deformity 4. Treatment of non-union, femoral neck…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0633-2021·2020-12-23
Maquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breach
Maquet Cardiovascular is recalling the HLS Set Advanced because of breaches in the product's sterility barrier. The device is used with the CARDIOHELP system for cardiac and pulmonary support.
Product
HLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Product Code/Part Number: 70105.2794 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0632-2021·2020-12-23
Maquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breaches
Maquet Cardiovascular is recalling HLS Set Advanced devices used for cardiac support due to breaches in the product's sterility barrier.
Product
HLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Number: 70105.2797 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0617-2021·2020-12-23
Biomet Cannulated Screw System Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of cannulated screw systems because a breach in the sterile packaging seal could lead to loss of sterility.
Product
4.0/5.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009810, 110009821, 110009825, 110009852 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0628-2021·2020-12-23
Biomet Hip Prosthesis Recall for Potential Sterile Seal Breach
Biomet is recalling specific lots of RINGLOC BIPOLAR Hip System components due to a potential breach in the sterile seal, which could lead to loss of sterility.
Product
RINGLOC BIPOLAR Hip System Bi Polar Locking Ring, Item number 11-165304 - Product Usage: Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, Prosthesis, Hip…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0588-2021·2020-12-23
BD PrecisionGlide Needles Recalled Due to Blood Contamination
Becton Dickinson is recalling BD PrecisionGlide needles because blood was found on the cannulas, posing a potential infection risk if not noticed by clinicians.
Product
BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V810000·2020-12-23
International DuraStar and WorkStar Engine Control Software Defect Recall
Navistar recalls 17,213 2014-2021 International commercial trucks with an engine control defect. The software flaw can cause unexpected vehicle movement when parked with the PTO engaged, risking crashes and injury.
Product
INTERNATIONAL — INTERNATIONAL MV, DURASTAR, WORKSTAR, HV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0636-2021·2020-12-23
Kowa VK-2s Software Recall for Potential Patient Data Deletion
Kowa Optimed Inc is recalling VK-2s software installed on nonmyd WX Retinal Cameras because a defect may cause the deletion of all patient information, potentially delaying treatment.
Product
Kowa VK-2s software Version 10.0.4.0, Product code 04987646809500 installed on Kowa nonmyd WX Retinal Cameras - Product Usage: is indicated for acquiring, displaying and storing image data from KOWA s mydriatic and non-mydriatic ophthalmic cameras.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V811000·2020-12-23
GM Recalls Bolt EV and Other Vehicles for Seat Belt Attachment Defect
General Motors is recalling multiple 2020-2021 vehicles due to incorrect bolts used to secure seat belts. Improperly fastened seat belts may fail to properly restrain occupants in a crash.
Product
CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE NA, COLORADO, SILVERADO 3500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0565-2021·2020-12-23
Terumo Capiox FX25 Advance Oxygenator Recall for Configuration Error
Terumo is recalling Capiox FX25 Advance Oxygenators because they may have the incorrect East or West configuration. The recall affects 5,079 units distributed in the US and abroad.
Product
(1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advance, Sterile Catalog Number: 3CX*FX25RWC (2) Capiox FX25 (East) Advance Oxygenator - FX25 with right port, 4-liter Reservoir, XC modified to Advance Catalog Number…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0152-2021·2020-12-23
Taro Recalls HEB Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling HEB Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
HEB — HEB (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0634-2021·2020-12-23
Roche Recalls Tina-quant C-Reactive Protein Gen.3 Reagents Due to Cross-Contamination
Roche is recalling Tina-quant C-Reactive Protein Gen.3 reagents due to cross-contamination causing invalid calibrations and low quality control recovery.
Product
Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative determination of CRP in human serum and plasma on Roche automated clinical chemistry analyzers.
Category
Medical Device
Distribution
Distributed nationwide