The Recall Desk

State

Idaho product recalls

72,940 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total
3,517
Critical
364
Severe
1,023
Most recent
2026-09-06

Of the 3,517 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 1,023 (29%) are Severe.

These figures cover only the 3,517 recalls whose distribution notice names Idaho specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3751–3775 of 76457

  • HighCPSC·26192·2026-01-15

    Adirondack patio chairs recalled because they can crack and collapse

    About 6,100 Adams RealComfort and StyleWell Adirondack patio chairs are being recalled because the chairs can crack and collapse, posing injury and fall hazards.

    Product
    Adams RealComfort and StyleWell Adirondack Patio Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26194·2026-01-15

    HEZI power strips recalled over an ungrounded metal enclosure

    About 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.

    Product
    HEZI Branded Power Strips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0289-2026·2026-01-14

    ClearLife allergy nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.

    Product
    CLEARLIFE EXTRA STRENGTH — CLEARLIFE EXTRA STRENGTH (ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1000-2026·2026-01-14

    Organ recovery packs recalled as not suitable for organ transplant

    AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1001-2026·2026-01-14

    Organ recovery surgical packs recalled as not suitable for organ transplant

    AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1002-2026·2026-01-14

    Mini Plus surgical kits recalled as not suitable for organ transplant

    AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0288-2026·2026-01-14

    ReBoost nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.

    Product
    REBOOST — REBOOST (SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0375-2026·2026-01-14

    Frozen tater tots recalled over clear hard plastic fragments

    McCain Foods USA is recalling 21,256 cases of Ore-Ida Tater Tots shaped potatoes over clear hard plastic fragments.

    Product
    Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag per case. Net wt. 30 lbs. UPC 1 00 72714 00215 8. McCain Foodservice Solutions.
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-1035-2026·2026-01-14

    Oxygen masks recalled after complaints of tubing disconnecting during use

    Medline is recalling 1,611,081 Hudson RCI medium concentration oxygen masks after multiple complaints of tubing disconnecting, which may lead to shortness of breath and hypoxia.

    Product
    Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED CONC,SHORT,PEDI,7' TUB SC; HUD1042 O2 MASK,MED CONC,PEDI,7' TUB SC; HUD1930 O2 MASK,MED CONC,ADULT,7' TUB UC; HUDRHO41U MASK,OXYGEN,MEDIUM-CONCENTRAT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1033-2026·2026-01-14

    Telemetry monitors recalled over a failure to reconnect between access points

    Philips North America is recalling 13,470 Smart-hopping 2.0 AP 1.4 GHz patient monitors because the MX40 could not reconnect to the PIC iX when signal strength changed quickly.

    Product
    Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1019-2026·2026-01-14

    C. difficile assay recalled over declining performance and false negative results

    Meridian Bioscience is recalling 211 units of the Revogene C. difficile assay because affected lots show a decline in performance over time, which may lead to false-negative results.

    Product
    Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0379-2026·2026-01-14

    Frozen raw shrimp recalled over possible contamination with Cesium-137

    Direct Source Seafood is recalling 1,800 cases of waterfront BISTRO frozen raw shrimp, sold alongside Market 32 brand shrimp, because the shrimp may be contaminated with Cesium-137.

    Product
    waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Product is packaged in white flexible plastic pouch with multicolored labeling. UPC is 0 21130 13224 9. Product of Indonesia. DISTRIBUTED BY LUCERNE FOODS, INC. P.O
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-1032-2026·2026-01-14

    Emergency call stations recalled over missing low battery alerts

    Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.

    Product
    Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1034-2026·2026-01-14

    Head fixation devices recalled because a torque screw may crack or separate

    IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.

    Product
    Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000, 113803-000, 113803-600, 113802-000, 113802-600 Software Version: Not Applicable Product Description: The HFD100 Head Fixation Device provides rigid skeletal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1027-2026·2026-01-14

    Patient monitors recalled over unvalidated intracranial and bladder pressure measurements

    Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.

    Product
    Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1009-2026·2026-01-14

    Thyroid receptor immunoassay recalled over variable results across instrument platforms

    Roche Diagnostics is recalling 1,300 Elecsys Anti-TSHR cassettes because results vary by instrument platform and calibrator lots vary, which may lead to incorrect diagnosis or treatment.

    Product
    The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and electrochemiluminescence detection. Patient serum sample is incubated with pretreatment reagent PT1 and the reconstituted PT2 containing a pre-formed immunocompl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0380-2026·2026-01-14

    Market 32 frozen raw shrimp recalled over possible Cesium-137 contamination

    Direct Source Seafood is recalling 3,290 cases of Market 32 by Price Chopper frozen raw shrimp because the shrimp may be contaminated with Cesium-137.

    Product
    MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on 26/30 count per pound. Net 16oz. Product is packaged in a clear flexible plastic package with brown label and blue and green printing. UPC is 0 41735 01358 3. Product of Indonesia. PROUDLY DISTRIBUTED BY PR
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-1028-2026·2026-01-14

    Medication dispensing servers recalled over delayed updates from enterprise systems

    CareFusion 303 is recalling 2,079 BD Pyxis ES Enterprise Server systems over a software issue that may result in equipment not receiving timely updates of patient or medication information.

    Product
    BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03, 139676-01, 139421-01, 139420-01, 139419-01, 139419-02, 139673-01, 137081-01, 136451-01, 136451-02, 136450-01, 136450-02, 136449-01, 136449-02, 134148-01, 133760
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1031-2026·2026-01-14

    Arial call stations recalled over a firmware issue affecting battery alerts

    Securitas Healthcare is recalling 5,627 Arial 900 MHz Call Stations, model CSK200-900, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.

    Product
    Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0392-2026·2026-01-14

    Italian parsley recalled over the pathogen Cyclospora cayetanensis

    MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.

    Product
    Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0376-2026·2026-01-14

    Frozen tater barrels recalled over clear hard plastic fragments

    McCain Foods USA is recalling 17,597 cases of Sysco Imperial Potato Tater Barrel over clear hard plastic fragments.

    Product
    Sysco Imperial Potato Tater Barrel, item number 1000006067. Frozen potato product is packaged in 6/5 lb. clear unlabeled poly bags per case. UPC 1 07 34730 62740 0. Distributed by Sysco Corporation, Houston, TX. Product of U.S.A.
    Category
    Food
    Distribution
    26 states