The Recall Desk

State

Utah product recalls

73,824 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.

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45601–45625 of 78740

  • HighFDA (Devices)·Z-2682-2017·2017-07-19

    ICU Recalls Plum A+ Infusion Systems Due to Battery Error

    ICU is recalling 7,351 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2569-2017·2017-07-19

    National Fish & Seafood Recalls Perch Fillets for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Perch Fillets because the product may contain undeclared milk.

    Product
    SCHOONER PRE-COOKED CRUNCHY PERCH FILLETS 12/16 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2728-2017·2017-07-19

    Natus Neurology Recalls Elite Obstetric Probes Due to Excessive Background Noise

    Natus Neurology is recalling 2,335 Elite Obstetric probes because excessive background noise may mask heart rate and blood flow sounds.

    Product
    Nicolet¿ Elite¿ 3 MHz OB Probe, Model #: X1L001, Catalog Code: N300. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2556-2017·2017-07-19

    Murrys Pre-Cooked Steaks Recalled for Undeclared Milk Allergen

    National Fish & Seafood, Inc. is recalling specific lots of Murrys Pre-Cooked Steaks because the product may contain undeclared milk.

    Product
    MURRYS PRE COOKED STEAKS 6/2.4 3.2 OZ, 9/4 3.2 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2680-2017·2017-07-19

    ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption

    ICU is recalling 7,848 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2572-2017·2017-07-19

    Schooner Pre-Cooked Crunchy Whiting Fillets Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Whiting Fillets because the product may contain undeclared milk.

    Product
    SCHOONER PRE-COOKED CRUNCHY WHITING FILLETS 1/10 LB and SCHOONER PRE-COOKED CRUNCHY WHITING FILLETS 12/16 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2678-2017·2017-07-19

    ICU Recalls 214 Plum A+ Infusion Systems Due to Battery Error

    ICU is recalling 214 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2548-2017·2017-07-19

    Lil Fisherman Pollock Sticks Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Lil Fisherman Pre Cooked Pollock Sticks because the product may contain undeclared milk.

    Product
    LIL FISHERMAN PRE COOKED POLLOCK STICKS 1 OZ GRADE A 10 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2691-2017·2017-07-19

    St. Jude Medical Recalls Proclaim 5 Elite Implantable Pulse Generators

    St. Jude Medical is recalling 8,780 Proclaim 5 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.

    Product
    Proclaim 5 Elite, implantable Pulse Generator, REF 3660, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2707-2017·2017-07-19

    Merge Healthcare Recalls Schiller PB 1000 Patient Data Module

    Merge Healthcare is recalling 555 Schiller PB 1000 Patient Data Modules because the analog output may not accurately reflect the pressure waveform used for fractional flow reserve calculations.

    Product
    The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM), a major component of the Merge Hemo software.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2017·2017-07-19

    Natus Neurology Recalls Elite 2 MHz OB Probes Due to Excessive Noise

    Natus Neurology is recalling 2,335 Elite 2 MHz OB probes because excessive background noise may mask the user's ability to hear heart rate or blood flow.

    Product
    Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2466-2017·2017-07-19

    3CS Organics Recalls Unapproved Holle Goat Milk Infant Formula

    3CS Organics LLC is recalling Holle goat milk infant formula products that are not FDA approved and lack English labeling.

    Product
    HOLLE Bio Lait Pour Nourrissons Au Lait De Chevre, Zuigelingenmelk OP Geitenmelbasis, 1, 400g (4/case), HOLLE Bio-Flogemilch Auf Ziegenmilchbasis, 1, 400g (4/case), HOLLE Bio-Folgenmilch Auf Ziegenmilchbasis, 3, 400g (4/case), HOLLE Bio-Folgemich, 2, 600g (3bx/case), HOLLE…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2546-2017·2017-07-19

    Lil Fisherman Pollock Nuggets Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Lil Fisherman Pre Cooked Pollock Nuggets because they may contain undeclared milk.

    Product
    LIL FISHERMAN PRE COOKED POLLOCK NUGGETS 1 OZ PUFI 1/10 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-2551-2017·2017-07-19

    Matlaws Buffalo Popcorn Shrimp Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Matlaws Buffalo Popcorn Shrimp because the product may contain undeclared milk.

    Product
    MATLAWS P/C BRD BUFFALO POPCORN SHRIMP 12/8 OZ
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-2570-2017·2017-07-19

    Schooner Pre-Cooked Cod Fillets Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Schooner Pre-Cooked Crunchy Styled Cod Fillets because the product may contain undeclared milk.

    Product
    SCHOONER PRE-COOKED CRUNCHY STYLED COD FILLET 10 LB and SCHOONER PRE-COOKED CRUNCHY STYLED COD FILLETS 12/16 OZ
    Category
    Food
    Distribution
    24 states
  • HighNHTSA·17V459000·2017-07-19

    Carry-On Trailer Recalls 2017 Models Due to Electric Brake Defect

    Carry-On Trailer is recalling 2017 Utility, Dump, and Enclosed trailers because a faulty breakaway box light may cause the circuit board to fail, increasing crash risk.

    Product
    CARRY-ON TRAILER — CARRY-ON TRAILER ENCLOSED, UTILITY, DUMP
    Category
    Vehicle
    Distribution
    Distributed nationwide