The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

1951–1975 of 27346

  • HighFDA (Devices)·Z-0233-2026·2025-10-29

    Oral thermometer probes recalled after being programmed with rectal configuration

    Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.

    Product
    Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0300-2026·2025-10-29

    Millenium MPS gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 54 Millenium MPS gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MPS; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0232-2026·2025-10-29

    Insulin pumps recalled over software defect causing unexpected correction bolus

    Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.

    Product
    t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0241-2026·2025-10-29

    Interventional fluoroscopy systems recalled over control board corrosion affecting imaging

    Philips is recalling 29 Zenition 50 interventional fluoroscopic X-ray systems because corrosion of the image intensifier television control board may cause loss of imaging or poor image quality.

    Product
    Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0295-2026·2025-10-29

    Elscint Helix gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling three Elscint Helix gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Helix; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0238-2026·2025-10-29

    BD MAX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2026·2025-10-29

    Maxicam gamma cameras recalled over risk of detector falling from mount

    GE HealthCare is recalling 37 Maxicam gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Maxicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0210-2026·2025-10-29

    Dual lumen stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 16 Fr/Ch (5.3 mm) 266148 Salem Sump" Stomach Tube, Dual Lumen with Anti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0237-2026·2025-10-29

    Blood culture systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0301-2026·2025-10-29

    Optima NX gamma camera recalled over risk of detector falling

    GE HealthCare is recalling one Optima NX gamma camera because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Optima NX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0239-2026·2025-10-29

    Automated microbiology systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0236-2026·2025-10-29

    BACTEC FX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0240-2026·2025-10-29

    Veritor Connect software recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0302-2026·2025-10-29

    Sopha Medical Vision cameras recalled over risk of detector falling

    GE HealthCare is recalling 205 Sopha Medical Vision gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Sopha Medical Vision (SMV) DSXi/DST-XLi,/ DST-XL/ DSTi; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0298-2026·2025-10-29

    Millenium Myosight gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 82 Millenium Myosight gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium Myosight; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0213-2026·2025-10-29

    Central stations recalled over reboot loop that halts patient monitoring

    GE HealthCare is recalling 173 Carescape Central Stations running software V3.0.5 because the system can enter a continuous reboot cycle, losing central monitoring of connected patients.

    Product
    GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5; Part Number 5867474-04; Medical Display, cathode ray tube
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0290-2026·2025-10-29

    Elscint Cardial gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 11 Elscint Cardial gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Cardial; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0297-2026·2025-10-29

    Millenium gamma cameras recalled over risk of detector falling from mount

    GE HealthCare is recalling 1,386 Millenium MG/MC gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MG/MC; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0212-2026·2025-10-29

    AC joint fixation implants recalled over potentially missing slotted button assembly

    Biomet is recalling 98 ZipTight Acute AC Joint Implants from one lot because of the potential for a missing slotted button assembly.

    Product
    BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0211-2026·2025-10-29

    Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0234-2026·2025-10-29

    Prefilled saline flush syringes recalled over sodium chloride concentration shortfall

    Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.

    Product
    Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0291-2026·2025-10-29

    Elscint 4XX gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 64 Elscint Model 4XX gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Model 4XX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0294-2026·2025-10-29

    Elscint Varicam gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 15 Elscint Varicam gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Varicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0227-2026·2025-10-29

    Bipolar hip heads recalled downstream after femoral components failed transit testing

    Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.

    Product
    iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0299-2026·2025-10-29

    Millenium MPR gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 292 Millenium MPR gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MPR; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states