The Recall Desk

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.

43626–43650 of 78733

  • HighFDA (Devices)·Z-0207-2018·2017-12-13

    BD Precision Glide Needles Recalled for Hub Damage and Leakage

    Becton Dickinson is recalling 2,598,000 BD Precision Glide Needles due to hub damage that can cause breakage or leakage during use.

    Product
    BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0193-2018·2017-12-13

    Pro-Med Instruments Recalls DORO Sterile Disposable Skull Pins Due to Breakage

    Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.

    Product
    pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), STERILE R, Rx ONLY The DORO(R) Skull Pins are inserted into the receptacles of the skull clamp and fixate the head during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0197-2018·2017-12-13

    Roche Recalls Accu-Chek Connect App Due to Bolus Advisor Bug

    Roche Diabetes Care is recalling the Accu-Chek Connect app because a bug in the Bolus Advisor feature may prevent correction bolus advice from being available for recent glucose readings.

    Product
    Accu-Chek Connect diabetes management software app, Catalog number 07562462001 / GTIN number 00365702700000, Catalog number 07250452001 / GTIN number 00365702700017 The Accu-Chek Connect Diabetes Management App is indicated as an aid in the treatment of diabetes. The software…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0195-2018·2017-12-13

    ICU Medical Recalls MedNet Medication Management Suite Software

    ICU Medical Inc is recalling MedNet 6.1 and 6.21 software because it may alter piggyback medication settings without user notice.

    Product
    ICU Mednet(TM) Medication Management Suite 6.1 and 6.21, Product Code/List Numbers: (a) 16037-64-01; MedNet 6.1 b) 16037-64-02; MedNet 6.1 c) 16037-64-03; MedNet 6.1 d) 16037-64-04; MedNet 6.21 The ICU Medical MedNet Medication Management Suite (MMS) is intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0211-2018·2017-12-13

    Biosense Webster Recalls PENTARAY NAV High-Density Mapping Catheters

    Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because the instructions for use were updated to indicate they should not be used in patients with prosthetic valves.

    Product
    PENTARAY NAV High-Density Mapping Catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0199-2018·2017-12-13

    DeRoyal Surgical Kits Recalled for Incorrect Expiration Date on Prep Pads

    DeRoyal is recalling sterile custom surgical kits containing Medline Aplicare Povidone Iodine Prep Pads due to incorrect expiration dates.

    Product
    DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep Pads: a) Incision and Drainage Tray, REF 47-763.04 b) Incision and Drainage Tray, REF 47-763.06 c) Incision and Drainage Tray, REF 47-763.07 d) Cricothyreotomy Ambulance Kit, REF 89-6752.01 e)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0206-2018·2017-12-13

    Novo Nordisk Recalls Dial-A-Dose Insulin Pen Cartridge Holders

    Novo Nordisk is recalling specific batches of Dial-A-Dose insulin pen cartridge holders because they may crack or break when exposed to certain cleaning agents.

    Product
    Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product Usage: The NovoPen Echo¿ is a re-usable pen injector for single patient use by diabetics for the self injection of a desired dose of insulin. The pen injector uses Penfill 3 mL cartridge of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0204-2018·2017-12-13

    FDA Recalls Two Unapproved Morning Life Air Compression Devices

    Won Industry Co. is recalling two Morning Life air compression devices because they were distributed without FDA approval and have incorrect air compression settings.

    Product
    Morning Life, Model WIC2008S & WIC2008, UDI 8809293 870336 Product Usage: Intended for limb massage utilizing air compression. It is specially designed to improve venous and lymphatic circulation by compressing and releasing air pressure programmed on the device. It helps to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0203-2018·2017-12-13

    Fukuda Denshi Patient Monitor Recall for Damaged Lithium-Ion Capacitor

    Fukuda Denshi is recalling DS-8100M and DS-8100N patient monitors because a damaged lithium-ion capacitor may cause a short-term battery error message.

    Product
    Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage: Use of the Fukuda Denshi DynaScope Model DS-8100N/8100M Patient Monitor is indicated in those situations where observation of one or more of the following parameters on an individual patient may be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0212-2018·2017-12-13

    Biosense Webster Recalls PENTARAY NAV Mapping Catheters Due to Labeling Update

    Biosense Webster is recalling 73,796 PENTARAY NAV High-Density Mapping Catheters to update contraindication language in the Instructions For Use regarding prosthetic valves.

    Product
    PENTARAY NAV High-Density Mapping Catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V798000·2017-12-12

    Micro Bird G5 School Bus Recall for Roof Crush Risk

    Micro Bird is recalling 2006-2017 G5 school buses because the roof may crush excessively in a rollover, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V797000·2017-12-12

    Newmar Recalls 2018 Bay Star Motorhomes for Lighting Defects

    Newmar is recalling 194 2018 Bay Star and Bay Star Sport motorhomes because front side marker lights may be disconnected and low beams may fail to illuminate with high beams.

    Product
    NEWMAR — NEWMAR BAY STAR SPORT, BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V788000·2017-12-11

    Ford Ranger Recall: Passenger Air Bag Inflator Rupture Risk

    Ford is recalling 2004-2006 Ranger trucks because the passenger air bag inflator may rupture during deployment, sending metal fragments into the vehicle.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V796000·2017-12-11

    Aston Martin Recalls 3,493 Vehicles for Transmission Park Pawl Defect

    Aston Martin is recalling 3,493 vehicles because a communication error may prevent the transmission park pawl from engaging, increasing the risk of the vehicle rolling unexpectedly.

    Product
    ASTON MARTIN — ASTON MARTIN VIRAGE, DBS, DB9, RAPIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V787000·2017-12-11

    Ford Ranger Recall: Driver Air Bag Inflator Rupture Risk

    Ford is recalling 2004-2006 Ranger trucks to replace driver air bag inflators that may rupture during deployment, posing a risk of serious injury.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V795000·2017-12-11

    Aston Martin Recalls DB9 and DBS Vehicles for Battery Cable Fire Risk

    Aston Martin is recalling 2005-2009 DB9 and DBS vehicles because the battery supply cable may be damaged by the driver seat, creating a fire risk.

    Product
    ASTON MARTIN — ASTON MARTIN DB9, DBS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18057·2017-12-11

    Ravin Crossbows Recalls Arrow Nocks Due to Injury Hazard

    Ravin Crossbows is recalling approximately 220,000 white plastic arrow nocks because they may malfunction, posing an injury hazard to users.

    Product
    Ravin arrow nocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V792000·2017-12-11

    Navistar Recalls International Trucks Due to Fire Extinguisher Defect

    Navistar is recalling specific International trucks because the installed fire extinguishers may clog, require excessive force to activate, or detach, potentially causing injury or failing to suppress a fire.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, 9100I, 4900, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V791000·2017-12-08

    JH Global Recalls 2017 Star EV Sport 4+2 for Steering Defect

    JH Global is recalling 2017 Star EV Sport 4+2 vehicles because a casting problem may cause the tie rod to break, resulting in a loss of steering control.

    Product
    STAR EV — STAR EV SPORT 4+2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V789000·2017-12-08

    Grand Design Recalls 2017-2018 Travel Trailers Due to Tongue Jack Defect

    Grand Design is recalling 2017-2018 Reflection and Imagine travel trailers because a cracked touch pad on the power tongue jack may allow water entry, causing the jack to operate unintentionally.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE, REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide