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)

3126–3150 of 113831

  • SevereFDA (Devices)·Z-1589-2026·2026-04-08

    Impella purge cassettes recalled as Class I over purge leak risk

    Purge Cassettes sold within Impella Pump Sets and individually packaged are being recalled because of an increased risk of purge leaks with Generation 1 purge cassettes.

    Product
    Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding product codes. 1. Purge Cassette, 5 Pack; Product Code: 0043-0003. 2. Impella RP US Pump Set; Product Code: 004334. 3. Purge C
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0478-2026·2026-04-08

    Magnesium sulfate pouch recalled as Class I for containing tranexamic acid

    One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.

    Product
    MAGNESIUM SULFATE — MAGNESIUM SULFATE (MAGNESIUM SULFATE IN WATER FOR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1649-2026·2026-04-08

    Trilogy Evo Universal obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    Product
    Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0661-2026·2026-04-08

    Imu-Tek Colostrum-5 Powder Recalled Due to Under-Processing Risk

    Imu-Tek Animal Health has recalled Imu-Tek Colostrum-5 Powder because the product may be under-processed. The recalled lot was distributed across 29 states.

    Product
    Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band exterior seal, 24 ounces (680 grams) powder, 7 38654 00052 6, ImuTek Laboratories, Fort Collins
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Devices)·Z-1637-2026·2026-04-08

    Volara ventilator adapter recalled as Class I over desaturation and barotrauma

    Baxter is issuing an urgent correction for the Blue Ventilator Adapter Module used with the Volara system because home users may be unaware of possible oxygen desaturation or lung injury from overexpansion.

    Product
    Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·H-0640-2026·2026-04-08

    Spray Dried Dairy Powder recalled due to Salmonella contamination

    Lone Star Dairy Products LLC is recalling Spray Dried Dairy Powder in 25 kg bags and 1 metric ton totes due to Salmonella identification in finished product testing.

    Product
    Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1648-2026·2026-04-08

    Trilogy EV300 obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    Product
    Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1647-2026·2026-04-08

    Trilogy Evo O2 obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    Product
    Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1735-2026·2026-04-08

    Civco eTRAX 12G needle sensor may misreport needle tip position

    Civco is recalling the eTRAX Needle Sensor 12G for Aurora trackers because an inspection and programming error may cause the needle tip position to be incorrectly identified.

    Product
    eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1761-2026·2026-04-08

    Burlington Medical leg wraps may lose radiation attenuation over time

    Burlington Medical is recalling leg wraps because of the potential for attenuation degradation over time, decreasing the lifespan of the product.

    Product
    Burlington Medical, Leg Wraps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1757-2026·2026-04-08

    Burlington Medical wrap aprons may lose radiation attenuation over time

    Burlington Medical is recalling wrap aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Wrap Aprons.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0637-2026·2026-04-08

    Divided Sunset Multi Collagen Peptides Missing Allergen Labeling

    TG FOODS INC is recalling Divided Sunset Multi Collagen Peptides (8 oz) because the product contains eggshell membrane collagen and wild-caught marine collagen but fails to declare EGG and the specific fish species on the label.

    Product
    Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-1684-2026·2026-04-08

    CPX 4 tall height tissue expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth tall height range because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH, SCPX-123TH, SCPX-140TH, SCPX-146TH Smooth Tall Height Tissue Expander, 350cc, 450cc, 650cc, 750cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1677-2026·2026-04-08

    Philips Azurion 7 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0413-2026·2026-04-08

    GoodSense original formula eye drops recalled over sterility assurance

    GoodSense Eye Drops Original Formula, containing tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.

    Product
    GOODSENSE EYE DROPS ORIGINAL FORMULA — GOODSENSE EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1663-2026·2026-04-08

    Philips Allura Xper FD20 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1736-2026·2026-04-08

    Civco eTRAX 14G needle sensor may misreport needle tip position

    Civco is recalling the eTRAX Needle Sensor 14G for Aurora trackers because an inspection and programming error may cause the needle tip position to be incorrectly identified.

    Product
    eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1669-2026·2026-04-08

    Philips Allura Xper FD20/20 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/20; System Code: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1659-2026·2026-04-08

    Philips Allura Xper FD10C X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD10C; System Code: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1668-2026·2026-04-08

    Philips Allura Xper FD20/10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/10; System Code: 722029;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2026·2026-04-08

    Philips Azurion 7 B12 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2026·2026-04-08

    Oxoid Microbact Listeria kit may identify the incorrect organism

    Oxoid, part of Thermo Fisher Scientific, is recalling one lot of the Microbact 12L Listeria identification kit because it may identify the incorrect organism.

    Product
    OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1694-2026·2026-04-08

    Olympus SOLTIVE Premium laser power supply may fail producing smoke

    Olympus is recalling SOLTIVE Premium SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.

    Product
    Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1670-2026·2026-04-08

    Philips Allura Xper FD20/20 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/20 OR Table; System Code: 722039;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1685-2026·2026-04-08

    Artoura textured tissue expander infusion set needles may be blunt

    Mentor is recalling textured Artoura Breast Tissue Expanders with integral injection dome because the infusion sets may contain a dull or blunt needle tip.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,
    Category
    Medical Device
    Distribution
    Distributed nationwide