The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

2376–2400 of 52932

  • HighCPSC·26191·2026-01-15

    Crib mattresses recalled because they may not fit certain cribs

    About 1,500 KEAWIS crib mattresses are being recalled because they may not adequately fit certain play yards or non-full-sized cribs, creating gaps that pose an entrapment hazard.

    Product
    KEAWIS Crib Mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • 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
  • 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 (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-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-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-0354-2026·2026-01-14

    Spicy breakfast burritos recalled over foreign material in 93 units

    Fresh & Ready Foods is recalling 93 units of Sprig & Sprout Spicy Breakfast Burrito over foreign material.

    Product
    Spicy Breakfast Burrito, Sprig & Sprout brand, Ready to Eat. Refrigerated. Net wt. 9.1oz. UPC 100001000297, SS00297v02. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057.
    Category
    Food
    Distribution
    2 states
  • 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 (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 (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 (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
  • 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 (Food)·H-0356-2026·2026-01-14

    Breakfast tacos recalled over foreign material in 200 units

    Fresh & Ready Foods is recalling 200 units of Evergreen Refreshments Eggs Potatoes Cheese Tacos over foreign material.

    Product
    Eggs Potatoes Cheese Tacos, Evergreen Refreshments brand, Ready to Eat, Refrigerated. Net wt. 6.3 oz. UPC 100040103898, EG03698v01. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0408-2026·2026-01-14

    Distilled water recalled over a floating black foreign substance

    Meijer is recalling 38,043 gallons of Meijer Steam Distilled Water because of a floating black foreign substance in the product.

    Product
    Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC 041250841197, Dist. By Meijer Distribution, Inc. Grand Rapids, MI 49544, packed 4 per case
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0251-2026·2026-01-14

    Tri-Moxi intraocular injection recalled over glass-like particulate matter

    Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.

    Product
    Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0250-2026·2026-01-14

    Intraocular injection syringes recalled over glass-like particulate matter

    Imprimis NJOF is recalling 596 boxes containing 11,920 pre-filled syringes of Dexamethasone, Moxifloxacin and Ketorolac intraocular injection over glass-like particles.

    Product
    Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL, 0.4 mg/mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01.
    Category
    Drug
    Distribution
    Distributed nationwide