The Recall Desk

State

Utah product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49776–49800 of 78743

  • ModerateFDA (Drugs)·D-0076-2017·2016-10-19

    Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 3,270 syringes of morphine sulfate due to stability data that does not support the expiry date, posing a potential loss of potency.

    Product
    morphine Sulfate, 0.5 mg per mL, in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 1 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0035-2017·2016-10-19

    Pharmedium Recalls Fentanyl Syringes Due to Potential Loss of Potency

    Pharmedium Services is recalling 8,955 syringes of fentanyl citrate because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3174.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0066-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 830 syringes of lidocaine HCl, 2%, preservative-free, because stability data does not support the expiry dates, posing a risk of potential loss of potency.

    Product
    lidocaine HCl, 2%, Preservative Free, Total Volume 2mL, Product code 2R3323, NDC 61553-323-79
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0054-2017·2016-10-19

    Pharmedium Recalls Ketamine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 1,500 syringes of ketamine HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    ketamine HCl, 10 mg per mL, 50 mg per 5 mL, 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3320.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0044-2017·2016-10-19

    Pharmedium Recalls Glycopyrrolate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 16,366 syringes of glycopyrrolate because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    glycopyrrolate, 0.2 mg per mL, 0.6 mg per 3 mL, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3217.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0063-2017·2016-10-19

    Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 5,900 syringes of lidocaine HCl 1% because stability data does not support the expiry dates, posing a risk of loss of potency.

    Product
    lidocaine HCl, 1%, in 0.9% Sodium Chloride, Preservative Free, Total Volume 1 mL in a syringe, Rx only, PharMEDium, Product code 2R3345.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2017·2016-10-19

    Pharmedium Recalls Ketamine HCl Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 9,101 syringes of ketamine HCl because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    ketamine HCl, 10 mg per mL, 20 mg per 2 mL, in 0.9% Sodium Chloride, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3330.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0083-2017·2016-10-19

    Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Concerns

    Pharmedium Services, LLC is recalling specific lots of neostigmine methylsulfate syringes because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    neostigmine Methylsulfate, 1 mg per mL, 2 mg per 2 mL, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3550.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0082-2017·2016-10-19

    Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 2,105 syringes of neostigmine methylsulfate because stability data does not support the expiration dates, posing a risk of reduced potency.

    Product
    neostigmine Methylsulfate, 1 mg per mL, 5 mg per 5 mL, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3326.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0065-2017·2016-10-19

    PharMEDium Lidocaine Syringes Recalled for Potential Loss of Potency

    PharMEDium is recalling lidocaine HCl syringes because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    lidocaine HCl, 2%, 40 mg per 2 mL, 2 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3112.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0009-2017·2016-10-19

    Amerisource Health Services Recalls Paricalcitol Capsules Due to Impurities

    Amerisource Health Services is recalling 648 cartons of Paricalcitol Capsules, 1 mcg, due to failed impurities specifications.

    Product
    Paricalcitol Capsules, 1 mcg, packaged in 30 Capsules (5 x 6) per carton (NDC 60687-106-25); each blister card containing 6 individually blistered capsules (NDC 60687-106-95), Rx only, Distributed by: American Health Packaging, Columbus, OH, 43217.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0095-2017·2016-10-19

    Teva Recalls MitoXANTRONE Injection Due to Potential Impurity D Failure

    Teva Pharmaceuticals USA is recalling MitoXANTRONE Injection USP vials nationwide because they may fail to meet specifications for Impurity D throughout their shelf life.

    Product
    mitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-4685-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0057-2017·2016-10-19

    Circulatory Technology Recalls Better-Bladder Devices Due to Cosmetic Defects

    Circulatory Technology Inc is recalling 958 units of Better-Bladder devices with 14-inch tubing due to twisted or wrinkled balloon components.

    Product
    The Better-Bladder With 14" ID tubing, ITEM BB14, STERILE, Measure pressure noninvasively in the extracorporeal circuit and provide compliance in the venous line between the patient and the pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0098-2017·2016-10-19

    Dr. Reddy's Recalls ZENATANE Isotretinoin Capsules for Dissolution Failures

    Dr. Reddy's Laboratories is recalling ZENATANE (isotretinoin) 20 mg capsules because they failed to meet dissolution specifications. The recall covers 3,858 prescription packs distributed nationwide.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17017·2016-10-18

    3 Squares Rice and Slow Cookers Recalled for Fire and Shock Hazards

    Sherwood Marketing is recalling 3 Squares rice and slow cookers because improperly installed wiring can cause electrical shorting, posing fire and electric shock risks.

    Product
    3 Squares rice and slow cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V752000·2016-10-18

    Polaris Recalls 2016-2017 Slingshot Motorcycles for Brake Seal Defect

    Polaris is recalling 2016-2017 Slingshot motorcycles because an over-tightened brake pressure switch may leak fluid, reducing brake performance and increasing crash risk.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V751000·2016-10-18

    Forest River Surveyor Recalled for Incorrect Federal Tire Placard

    Forest River is recalling 2016-2017 Surveyor recreational vehicles because the Federal Placard lists incorrect tire and rim specifications, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17016·2016-10-18

    TUSA Recalls Diving Computers Due to Drowning and Injury Hazards

    TUSA is recalling about 175 DC Solar Link IQ1204 diving computers because they may malfunction and display incorrect readings, posing a drowning and injury hazard.

    Product
    Diving computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V749000·2016-10-18

    Forest River Recalls 2016-2017 StarTrans and Glaval Transit Buses

    Forest River is recalling 2016-2017 StarTrans and Glaval transit buses because the instrument cluster may display 'PARK' instead of 'BRAKE' during a brake malfunction, increasing crash risk.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS LEGACY, PS2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17009·2016-10-18

    Husqvarna Recalls Lawn Mowers Due to Laceration Hazard

    Husqvarna is recalling about 235,000 walk-behind gas-powered lawn mowers because the operator presence control bar can malfunction, causing the engine and blades to continue running and posing a laceration hazard.

    Product
    Lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V747000·2016-10-17

    BMW Recalls 2016-2017 Models for Driver Seat Belt Retraction Defect

    BMW is recalling approximately 15,455 vehicles because the driver's seat belt may not lock properly during a crash, increasing injury risk.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE X1, COOPER S, COOPER CONVERTIBLE, 528I
    Category
    Vehicle
    Distribution
    Distributed nationwide