The Recall Desk

State

Utah product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52026–52050 of 78749

  • ModerateFDA (Drugs)·D-1030-2016·2016-06-22

    Nostrum Recalls Nitrofurantoin Oral Suspension for Failed Dissolution Specifications

    Nostrum Laboratories is recalling Nitrofurantoin Oral Suspension because it failed to meet dissolution specifications. The recall covers 2,839 bottles distributed nationwide.

    Product
    Nitrofurantoin Oral Suspension, USP, 25 mg/5 mL, FOR ORAL USE ONLY, URINARY TRACT ANTIBACTERIAL, Rx Only , 240 mL bottle, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Mfg. by: Sun Pharmaceutical Industries, Inc., Bryan, Ohio 43506, NDC 57664-239-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1038-2016·2016-06-22

    Par Pharmaceutical Recalls Pramipexole Dihydrochloride Extended Release Tablets

    Par Pharmaceutical is recalling Pramipexole Dihydrochloride Extended Release tablets because they contain a known impurity above approved specification levels.

    Product
    Pramipexole Dihydrochloride Extended Release Tablets, 0.375 mg, Rx Only, 30 count bottles, Manufactured By: Par Pharmaceutical Companies, Inc., Chestnut Ridge, NY 10977, NDC 10370-251-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1984-2016·2016-06-22

    Navilyst Medical Recalls BioFlo PICC Catheters Due to Hemolysis Risk

    Navilyst Medical is recalling BioFlo PICC catheters manufactured before July 15, 2014, because they lack a specification change that reduces hemolysis during blood sampling.

    Product
    BioFlo PICC with ENDEXO and PASV Valve Technology, MST-45 Kit, 6F-55cm, UPN H965458440 , Rx ONLY The Xcela PICC with PASV, Xcela Hybrid PICC with PASV, BioFlo PICC with PASV and BioFlo Hybrid PICC with PASV are indicated for short or long-term peripheral access to the central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1035-2016·2016-06-22

    Valeant Recalls Chlordiazepoxide HCl/Clidinium Bromide Capsules Due to Impurities

    Valeant Pharmaceuticals is recalling specific lots of Chlordiazepoxide HCl/Clidinium Bromide capsules because they failed impurities and degradation specifications.

    Product
    Chlordiazepoxide HCl/Clidinium Bromide capsules, 5 /2.5 mg, 100-count bottle, Rx Only, Manufactured in Canada by: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1957-2016·2016-06-22

    Miami Fat Supply Recalls Red Head 2 Fat Harvesting Canisters

    Miami Fat Supply is recalling 443 Red Head 2 Reusable Fat Harvesting Canisters because they were marketed without FDA clearance and are not approved for multiple use.

    Product
    The Red Head 2 Reusable Fat Harvesting Canister, Product # RH-2, Non-Sterile. Intended for use in aspirating subcutaneous fatty tissue in patients desiring aesthetic body contouring and autologous fat collection.
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-1980-2016·2016-06-22

    Navilyst Medical Recalls Xcela Hybrid PICC Catheters Due to Hemolysis Risk

    Navilyst Medical is recalling 357 Xcela Hybrid PICC catheters manufactured before July 15, 2014, because they lack a specification change that reduces hemolysis during blood sampling.

    Product
    Xcela Hybrid PICC with PASV Valve Technology, Intermediate MST-45 Kit, 6F-55cm, UPN H965952440 & UPN H965952450, Rx ONLY The Xcela PICC with PASV, Xcela Hybrid PICC with PASV, BioFlo PICC with PASV and BioFlo Hybrid PICC with PASV are indicated for short or long-term peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1981-2016·2016-06-22

    Navilyst Medical Recalls BioFlo and Xcela PICC Catheters

    Navilyst Medical is recalling specific BioFlo and Xcela PICC catheters because they lack a manufacturing change that reduces hemolysis during blood sampling.

    Product
    BioFlo PICC with ENDEXO and PASV Valve Technology, Catheter Kit, 6F-55cm, UPN H965458410, Rx ONLY The Xcela PICC with PASV, Xcela Hybrid PICC with PASV, BioFlo PICC with PASV and BioFlo Hybrid PICC with PASV are indicated for short or long-term peripheral access to the central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2001-2016·2016-06-22

    Natus neoBLUE Phototherapy System Recall for Warning Label Update

    Natus Medical is recalling 13,541 neoBLUE Phototherapy systems to add a warning statement to the instructions and provide a laminated Quick Guide for each device.

    Product
    Natus neoBLUE Phototherapy system, Catalogue Part Number: 010066. Top Assembly Part Numbers: 001103, 001314, 002110, 040906, 040904, 040756, 040758, 040658, 040680. Product Usage: Used to provide treatment for neonatal hyperbilirubinemia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1031-2016·2016-06-22

    Galderma Recalls Doxycycline Capsules Due to Missing Lot and Expiration Dates

    Galderma Laboratories is recalling Doxycycline USP Capsules 40 mg because some bottles are missing lot numbers or expiration dates.

    Product
    Doxycycline, USP Capsules 40 mg, Packaged in 30 ct Bottles, Rx Only. Marketed by: Prasco Laboratories, Mason, OH 45040 USA, Manufactured by: Catalent Pharma Solutions, LLC, Winchester, Kentucky 40391. NDC: 66993-815-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1034-2016·2016-06-22

    Valeant Recalls Librax Capsules Due to Failed Impurity Specifications

    Valeant Pharmaceuticals is recalling specific lots of Librax capsules because they failed impurity and degradation specifications.

    Product
    LIBRAX — LIBRAX (CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1948-2016·2016-06-22

    Leica Biosystems Recalls Ariol Automated Scanning Microscopes Due to Software Issue

    Leica Biosystems Richmond Inc. is recalling 33 Ariol automated scanning microscope systems because a manufacturing error resulted in an improperly activated Windows 7 operating system.

    Product
    Ariol is an automated scanning microscope and image analysis system. It is intended for in vitro diagnostic use as an aid to the pathologist in the detection, classification, and counting of cells of interest based on particular color, intensity, size, pattern, and shape.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1036-2016·2016-06-22

    Sandoz Recalls Lisinopril Tablets Due to Missing Package Insert

    Sandoz Inc is recalling 3,048 bottles of Lisinopril Tablets USP, 30 mg, because the package insert is incorrect or missing.

    Product
    Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V450000·2016-06-21

    Forest River Recalls 2016-2017 Flagstaff and Work N' Play Trailers

    Forest River is recalling 2016-2017 Flagstaff and Work N' Play trailers because a propane regulator sight glass may crack, allowing gas to leak and potentially cause a fire.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, WORK AND PLAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V452000·2016-06-21

    Navistar Recalls 2016 IC Bus RE School Buses for Seat Defect

    Navistar is recalling 2016 IC Bus RE school buses because child seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.

    Product
    IC BUS — IC BUS RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16199·2016-06-21

    Tommee Tippee Electric Bottle and Food Warmers Recalled for Fire Hazard

    Mayborn USA is recalling about 255,000 Tommee Tippee electric bottle and food warmers due to a fire hazard. The units can overheat, melt, smoke, and catch fire.

    Product
    Electric bottle and food warmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V449000·2016-06-21

    GM Recalls 2016 Chevrolet Equinox and GMC Terrain for Incorrect Tire Labels

    General Motors is recalling specific 2016 Chevrolet Equinox and GMC Terrain vehicles because their certification labels may display incorrect tire and rim size information.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V451000·2016-06-21

    Gillig Recalls 2012-2016 Low Floor Vehicles Due to Flashing Brake Lights

    Gillig is recalling 112 model year 2012-2016 Low Floor vehicles because the rear brake lights may flash inadvertently, which could confuse other drivers and increase crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V453000·2016-06-21

    Navistar Recalls 2017 International Trucks Due to Engine Stall Risk

    Navistar is recalling 1,191 model year 2017 International trucks because an electrical short in the engine control module can cause the engine to stall without restarting.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, PAYSTAR, HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V447000·2016-06-20

    Eldorado Shuttle Buses Recalled for Electrical Component Fire Risk

    Eldorado is recalling 2016 Aerotech, Aero Elite, and Advantage shuttle buses because a component in the electrical power distribution center may break, causing electrical arcing and increasing the risk of fire.

    Product
    ELDORADO — ELDORADO AERO ELITE, ADVANTAGE, AEROTECH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E058000·2016-06-20

    Speedtech Recalls Nitrous Solenoid Valves Due to Welding Defect

    Speedtech LLC is recalling Nitrous Solenoid Valves used in drag racing nitrous oxide systems because improper welding may cause the valve to separate and eject the piston under pressure.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·051-2016·2016-06-18

    GNP Company Recalls Chicken Products Due To Foreign Matter Contamination

    GNP Company is recalling approximately 55,608 pounds of chicken products that may be contaminated with sand and black soil. No illnesses have been reported.

    Product
    Pilgrim's Pride Corporation — GNP Company Recalls Chicken Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V446000·2016-06-17

    Indian Recalls 2014-2016 Motorcycles Due to Fire Risk

    Indian Motorcycle is recalling 2014-2016 models because engine misfires can raise exhaust temperatures, increasing the risk of fire.

    Product
    INDIAN — INDIAN CHIEF CLASSIC, CHIEFTAIN, ROADMASTER, VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V441000·2016-06-16

    Eldorado Amerivan 10 Recall for Fuel Line Leak Fire Risk

    Eldorado is recalling 2012-2016 Amerivan 10 vehicles because an improperly installed fuel line may leak and cause a fire.

    Product
    ELDORADO — ELDORADO AMERIVAN 10
    Category
    Vehicle
    Distribution
    Distributed nationwide