State

Utah product recalls

73,817 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,916
Critical: 524
Severe: 1,351
Most recent: 2026-11-04

Of the 4,916 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 1,351 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42026–42050 of 78733

HighFDA (Devices)·Z-1237-2018·2018-04-04
Signia Power Handle Recalled for Shutting Down During Surgical Use
Covidien LLC is recalling 2,121 Signia Power Handles because they reportedly shut down during use. The devices are used in various surgical procedures.
Product
Signia" Power Handle (SIGPHANDLE, SIGNVAL1 and SIGVAL20 - Kits) The Signia" Power Handle, when used with Endo GIA" single-use reloads and Endo GIA" single-use reloads with Tri-Staple" Technology, has applications in open and minimally invasive general abdominal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1219-2018·2018-04-04
DePuy Sigma HP Cemented Trochlear Implants Recalled for Elevated Revision Rates
DePuy Orthopaedics is recalling specific Sigma HP Cemented Trochlear Implants due to elevated revision rates identified during post-market surveillance.
Product
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP Cemented Trochlea Size 2 Narrow Left, Catalog Number: 102403200, GTIN: 10603295001621; (3) Sigma HP Cemented Trochlea Size 3 Narrow Left, Catalog Number: 102403300…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1215-2018·2018-04-04
Konica Minolta Sonimage HS1 Ultrasound Kit AC Adapter Recall
Konica Minolta is recalling 17 Sonimage HS1 Ultrasound Kit AC adapters due to a risk of circuit board breakage and smoke emission.
Product
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8AR, UDI: 04560141941588
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-1186-2018·2018-04-04
Cook Inc. Recalls IVF Intratubal Transfer Sets Due to Quality Testing Gaps
Cook Inc. is recalling specific lots of Echosight Jansen-Anderson Intratubal Transfer Sets because they were distributed without completed quality testing, posing a risk of nonviable embryos.
Product
Echosight Jansen-Anderson Intratubal Transfer Set, Catalog Number: K-J-JITS-572900, Global Product Number: G17946 Product Usage: Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1231-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL TROCH NAIL ST 13X180 130DG STRL TROCH NAIL ST 13X180 135DG STRL The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1259-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1233-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Screws
Zimmer Biomet is recalling ACE Trochanteric Nail System screws because a device performance review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN AR SCREW 65MM STERILE ATN AR SCREW 70MM STERILE ATN AR SCREW 75MM STERILE ATN AR SCREW 80MM STERILE ATN AR SCREW 85MM STERILE ATN AR SCREW 90MM STERILE ATN AR SCREW 95MM STERILE ATN AR SCREW 100MM STERILE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1214-2018·2018-04-04
Konica Minolta Recalls Sonimage HS1 Ultrasound Kit AC Adapters
Konica Minolta is recalling 30 Sonimage HS1 Ultrasound Kit AC adapters due to a risk of circuit board breakage and smoke emission.
Product
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: 1. A9RP, UDI: 04560141945463; 2. AAEU, UDI: 04560141946385; 3. A9RR, UDI: 04560141945470
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-1240-2018·2018-04-04
Zimmer Biomet Recalls Persona Partial Knee Spacer Blocks
Zimmer Biomet is recalling Persona Partial Knee Spacer Blocks because they may feel tight during trialing or appear loose in extension.
Product
Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1256-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 38mm, REF 804-07-380 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1184-2018·2018-04-04
Siemens Dimension Vista LOCI 8 Calibrator Recalled for Calibration Failures
Siemens Healthcare Diagnostics is recalling the Dimension Vista LOCI 8 Calibrator due to increased failed calibration events and negative bias in Estradiol assays.
Product
Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator is an in vitro diagnostic product for the calibration of follicle stimulating hormone (FSH), luteinizing hormone (LH), prolactin (PRL), and estradiol (E2) methods on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18E019000·2018-04-04
Badass Helmet Company Recalls Rogue Helmets for Safety Standard Non-Compliance
Badass Helmet Company is recalling Rogue helmets that may not adequately protect wearers in a crash, failing to meet Federal Motor Vehicle Safety Standard 218.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1176-2018·2018-04-04
ConMed Mini Infant Radiotranslucent Electrodes Recalled for Adhesive Conductivity Issues
ConMed is recalling 18,720 Mini Infant Radiotranslucent Electrodes because adhesive on contact wires may impede conductivity and cause failure.
Product
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1188-2018·2018-04-04
Cook Inc. Recalls IVF Embryo Transfer Sets Due to Quality Testing Gaps
Cook Inc. is recalling specific lots of IVF embryo transfer sets and catheters because they were distributed without completed quality testing, posing a risk of nonviable gametes or embryos.
Product
1. SMS Embryo Transfer Set, Catalog Number: K-J-SMS-571800, Global Product Number: G19182; 2. Guardia" Access Nano Embryo Transfer Catheter, Catalog Number: K-JETS-551910-L, Global Product Number: G24215; 3. Sydney IVF¿ Embryo Transfer Set, Product Number: K-JETS-7019-SIVF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1268-2018·2018-04-04
Roche cobas e 601 Immunoassay Analyzer Recalled for Questionable Results
Roche Diagnostics is recalling cobas e 601 Immunoassay Analyzers because complaints were received regarding questionable results caused by the use of 13 sample tubes without tube adapters.
Product
c6000, Chemistry (Photometric, Discrete), for clinical use. - cobas e 601 module: Immunoassay Analyzer, Catalog Numbers: 04745922001, 05036348001, 05860652001, 04745922692, 05036348001 & 05036348692
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1235-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System After Failed Performance Review
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 STER L H TROC NAIL 340X9X125 STER L H TROC NAIL 360X9X125 STER L H TROC NAIL 380X9X125 STER L H TROC NAIL 400X9X125 STER L H TROC NAIL 420X9X125 STER L H TROC NAIL 440X9X125 STER L H TROC NAIL 460X9X125 STER L H…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1180-2018·2018-04-04
BD Vacutainer Blood Collection Tubes Recalled for Residual Blood on Stopper
Becton Dickinson is recalling 1,976,000 BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tubes because increased residual blood was found on the top of the stopper well after venipuncture.
Product
BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1232-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC NAIL 125 DEG X 13MM STER TROC NAIL 130 DEG X 13MM STER TROC NAIL 135 DEG X 13MM The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1229-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a device performance review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STRL TROCH NAIL ST 11X180 130DG STRL TROCH NAIL ST 11X180 135DG STRL The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1258-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 46mm, REF 804-07-460 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1174-2018·2018-04-04
ConMed Mini Infant Radiotranslucent Electrodes Recalled for Adhesive Defect
ConMed is recalling 18,720 Mini Infant Radiotranslucent Electrodes because adhesive on contact wires may impede conductivity and cause device failure.
Product
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602 Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1181-2018·2018-04-04
Ohmeda Medical Recalls Rotating IV Poles Due to Fall Risk
Ohmeda Medical is recalling 1,179 rotating IV poles because they may fall, posing a risk of injury to patients, bystanders, or operators.
Product
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purchased to facilitate attachment and consolidation of patient equipment to one central patient care area. Devices commonly attached to IV poles…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1257-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 42mm, REF 804-07-420 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1234-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN LAG SCREW 65MM STERILE ATN LAG SCREW 70MM STERILE ATN LAG SCREW 75MM STERILE ATN LAG SCREW 80MM STERILE ATN LAG SCREW 85MM STERILE ATN LAG SCREW 90MM STERILE ATN LAG SCREW 95MM STERILE ATN LAG SCREW 100MM…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1185-2018·2018-04-04
Cook Inc. Recalls IVF Embryo Transfer Syringes Due to Quality Testing Gaps
Cook Inc. is recalling specific lots of Norm-Ject Tuberkulin Syringes used for IVF embryo transfer because they were distributed without completed quality testing.
Product
Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use
Category
Medical Device
Distribution
Distributed nationwide