The Recall Desk

State

Idaho product recalls

73,478 recalls have nationwide distribution and so reach Idaho. 3,523 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total
3,523
Critical
364
Severe
1,217
Most recent
2026-10-14

Of the 3,523 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,217 (35%) are Severe.

Which agencies issued them

These figures cover only the 3,523 recalls whose distribution notice names Idaho specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20926–20950 of 77001

  • HighFDA (Devices)·Z-1300-2022·2022-07-06

    Orthopedic Plates Recalled Due to Incorrect Etching and Mislabeling

    One lot of DVR Anatomic distal radius orthopedic plates was incorrectly etched during manufacturing and may have been placed into kits labeled as a different plate model. The affected plates were distributed to healthcare facilities nationwide.

    Product
    DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and osteotomies involving the distal radius.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22E054000·2022-07-06

    Cummins Recalls PD7000 Electric Drivetrains Due to Electrical Grounding Defect

    Cummins is recalling PD7000 Electric Drivetrains because an improperly grounded air compressor can cause electric shock. Owners will receive a free repair to install a ground strap.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1285-2022·2022-07-06

    Backup batteries in Avance CS2 anesthesia machines fail prematurely

    GE Healthcare is recalling backup batteries in Avance CS2 and CS2 Pro anesthesia machines manufactured after April 1, 2019. Batteries may fail earlier than expected, affecting approximately 6,600 devices worldwide.

    Product
    Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1309-2022·2022-07-06

    GCX Channel Mounting Accessory Screws May Loosen or Pull Out

    Skytron recalls its GCX Channel Mounting Accessory (model H8-300-40-A) because mounting screws may loosen or pull out when used as a monitor mount on surgical booms. Affected units were distributed worldwide.

    Product
    Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1169-2022·2022-07-06

    Methylphenidate Patch Recall: Defective Delivery System and Adhesive Issues

    Daytrana (methylphenidate) patches are being recalled due to ripping patches and poor adhesive transfer affecting drug delivery. This Class II recall involves 8,559 cartons distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1162-2022·2022-07-06

    Losartan Potassium tablets recalled for elevated AZIDO impurity

    PD-Rx Pharmaceuticals recalled Losartan Potassium 50 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. The recall affects 687 bottles across multiple lots.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1304-2022·2022-07-06

    HydroSurg Plus Laparoscopic Irrigator recalled for inability to irrigate

    Davol HydroSurg Plus Laparoscopic Irrigators cannot provide irrigation. The FDA issued a Class II recall affecting 4,780 units worldwide.

    Product
    HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction and Irrigation Tubing, Catalog number 0026880
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1295-2022·2022-07-06

    CV Minor Kit with Nonsterile Component Recalled for Contamination Risk

    ROi CPS LLC is recalling 180 CV Minor Kit units due to a nonsterile component accidentally packaged in the sterile kit, posing a contamination and infection risk.

    Product
    regard Item Number: 800774001, CV00979A - CV Minor Kit, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1284-2022·2022-07-06

    Tacrolimus Calibrator Set Recalled for Inaccurate Immunoassay Quantitation

    The QMS Tacrolimus Calibrator Set is recalled because calibrators recovered 82-94% of target values, causing inaccurate (over-quantitated) patient drug test results. This affects healthcare facilities in 20 US states and 9 countries.

    Product
    QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3 QMS TACROLIMUS CAL C 10015568-3 QMS TACROLIMUS CAL D 10015569-3 QMS TACROLIMUS CAL E 10015570-3 QMS TACROLIMUS CAL F 10015571-3
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1292-2022·2022-07-06

    Medical Device App Records Inaccurate Urinary Flow When Hearing Aids Active

    The ProudP Everyday Uroflow Tracker app may record lower-than-actual urination measurements when a hearing aid or AirPods Live Listen feature is active on the same iPhone, due to interference with the app's sound-based measurement system.

    Product
    ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1290-2022·2022-07-06

    Central venous catheter recalled for incorrect gravity flow rates

    Arrow International is recalling the Arrow Three-Lumen CVC due to incorrect gravity flow rates on the product lidstock. The defect may affect fluid and medication delivery through the catheter.

    Product
    Arrow Three-Lumen CVC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1161-2022·2022-07-06

    Losartan Potassium Tablets Recalled for Manufacturing Impurity Issues

    PD-Rx Pharmaceuticals recalls Losartan Potassium Tablets (25 mg, 90-tablet bottles) due to Current Good Manufacturing Practice deviations. Specific lot numbers contain AZIDO impurity levels above acceptable limits.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1163-2022·2022-07-06

    Losartan Potassium Tablets Recalled for Elevated AZIDO Impurity Levels

    PD-Rx Pharmaceuticals is recalling Losartan Potassium 100 mg tablets due to AZIDO impurity levels above acceptable limits detected during manufacturing. Approximately 1,320 bottles were distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V476000·2022-07-06

    2021–2022 Cargo trailers recalled for defective safety chains

    Forest River is recalling certain 2021–2022 Cargo Mate and Continental Cargo Trailers because safety chains don't meet weight rating specifications. A chain failure could cause the trailer to detach from the tow vehicle, increasing crash risk.

    Product
    CONTINENTAL CARGO — CONTINENTAL CARGO, CARGO MATE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1287-2022·2022-07-06

    Medline Pill Splitters recalled for unhinged lid exposing sharp blade

    Medline is recalling over 840,000 pill splitters due to a defect where the product lid can come unhinged, exposing a sharp blade and posing a laceration risk.

    Product
    Medline Pill Splitters; 1 each/box; 144 boxes/carton
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1296-2022·2022-07-06

    SOLTIVE SuperPulsed Laser Fibers recalled for model and size labeling mismatch

    Olympus is recalling certain SOLTIVE SuperPulsed Laser Fibers because device model and size may be mismatched between packaging and the actual device. This could result in the wrong laser fiber being used in medical procedures.

    Product
    SOLTIVE SuperPulsed Laser Fibers, Model# Labeled TFL-FBX150BS (Carton) - 150 Micron Ball Tip Single Use Fiber Model # Labeled TFL-FBX200S (Pouch) - 200 Micron Single Use Fiber Model # Labeled TFL-FBX200BS (Carton) - 200 Micron Ball Tip Single Use Fiber Model # Labeled…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2022·2022-07-06

    Artis Pheno fluoroscopic system may lose video display signals

    Siemens Artis Pheno fluoroscopic X-ray systems may lose video signals from the Large Display during procedures. In rare cases, both transceivers could fail, affecting displays in the examination and control rooms.

    Product
    Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1164-2022·2022-07-06

    FDA Recalls Losartan-Hydrochlorothiazide Tablets for Manufacturing Quality Deviations

    Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets (100 mg/25 mg) due to CGMP deviations and azido impurity levels exceeding acceptable limits. The affected lot is BLM2114A (expiration 07/2023) distributed nationwide.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V480000·2022-07-06

    Toyota 4Runner 2020-2022 Incorrect Tire Load Capacity Labels

    Southeast Toyota Distributors is recalling 2020-2022 Toyota 4Runners with 20-inch Black Gunner Wheels due to incorrect load capacity labels that could lead to vehicle overloading and increased crash risk.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1286-2022·2022-07-06

    Anesthesia device backup batteries may fail prematurely, GE Healthcare recalls

    GE Healthcare recalls backup batteries for anesthesia devices worldwide that may fail earlier than expected. The batteries are used in Avance CS2, Avance, Amingo, and Aespire View systems.

    Product
    Field replacement back up batteries distributed on or after April 1, 2019 for Avance CS2, Avance CS2 Pro, Avance, Amingo, Aespire View anesthesia devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1291-2022·2022-07-06

    Stryker INFINITY Resect Guide Recalled for Incorrect Color Coding

    Wright Medical is recalling 35 units of the Stryker INFINITY Resect Guide for INBONE Talus (Model #33620254) due to incorrect color coding. The color coding error could lead to misidentification and improper use during ankle surgery.

    Product
    Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1306-2022·2022-07-06

    NaviCare Nurse Call System Cancels Patient Calls During Wireless Use

    The NaviCare Nurse Call system software (versions 3.9.100-3.9.300) has a wireless integration defect causing patient calls to be canceled when answered on wireless phones. The issue affects 283 installations in the US and Canada.

    Product
    NaviCare Nurse Call/Voalte Nurse Call
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1310-2022·2022-07-06

    FDA Recalls TEG 5000 Fibrinogen Reagent Kits Due to Outdated Reference Ranges

    Haemonetics Corporation is recalling TEG 5000 Functional Fibrinogen Reagent kits because the reference ranges in the instructions have shifted. Clinicians using these outdated ranges could misdiagnose patients or fail to provide necessary treatment.

    Product
    TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2022·2022-07-06

    Surgical Light Paint Particles May Fall Into Operating Field

    Paint particles may detach from VOLISTA StandOP Surgical Lights and fall into the operating field during surgery, risking infection and organ irritation. Getinge Usa Sales Inc is recalling 337 affected units in the United States.

    Product
    VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP ARD568811961 VLT600DF AIM STP ARDVST229000A VST60SF AIM ARDVST229001A VST60DF AIM ARDVST229002A VST66SF AIM ARDVST229003A VST66DF AIM ARDVST229034A…
    Category
    Medical Device
    Distribution
    Distributed nationwide