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.

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3176–3200 of 113834

  • HighFDA (Devices)·Z-1706-2026·2026-04-08

    Medline bronchoscopy packs contain recalled Olympus biopsy valves shedding fragments

    Medline is recalling three bronchoscopy convenience kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.

    Product
    Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BRONCH PACK, DYNDA2861A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1737-2026·2026-04-08

    Civco eTRAX needle sensor may misreport needle tip position onscreen

    Civco is recalling the eTRAX Needle Sensor 16G for Aurora trackers because an inspection and programming error may cause the needle tip position to be incorrectly identified on the user interface.

    Product
    eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Drugs)·D-0408-2026·2026-04-08

    Amneal tramadol tablets failed nitrosamine impurity specification at stability

    Amneal Pharmaceuticals is recalling two lots of Tramadol Hydrochloride Tablets 50 mg after a nitrosamine impurity was found out of specification at the 24-month stability interval.

    Product
    TRAMADOL HYDROCHLORIDE — TRAMADOL HYDROCHLORIDE (TRAMADOL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1692-2026·2026-04-08

    Vue Motion V12 may display cine image frames out of sequence

    Philips is recalling Vue Motion V12 because mis-ordered frames during dynamic cine runs may cause image frames to display out of sequence.

    Product
    Vue Motion V12. Product Number: 1017979.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1681-2026·2026-04-08

    CPX 4 SILTEX low height expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the SILTEX low 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: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1698-2026·2026-04-08

    da Vinci mega needle driver recalled over broken or frayed cables

    Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1666-2026·2026-04-08

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

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

    Product
    ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0639-2026·2026-04-08

    Dumpling Party Tray Products Recalled for Glass Fragments

    JFE Franchising Inc is recalling three dumpling products due to possible glass fragments. Affected products include Dumpling Party Tray (20pcs and 40pcs) Vegetable varieties and Cheetos Flamin Hot Loaded Dumpling Vegetable.

    Product
    " Dumpling Party Tray (20pcs) Vegetable 13 oz 011110661173 " Dumpling Party Tray (40pcs) Vegetable 26 oz 011110661180 " Cheetos Flamin Hot Loaded Dumpling Vegetable 6oz 011110663474
    Category
    Food
    Distribution
    37 states
  • HighFDA (Devices)·Z-1688-2026·2026-04-08

    Stryker surgical light assembly may not support the ceiling cover weight

    Stryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System because the light assembly may not adequately support the weight of the ceiling cover.

    Product
    Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1662-2026·2026-04-08

    Philips Allura Xper FD10/10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1671-2026·2026-04-08

    Philips Allura Xper FD20/15 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/15; System Code: 722058;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1704-2026·2026-04-08

    Finesse BTK angioplasty balloon catheter may not meet burst specifications

    The Finesse BTK Multicath injectable angioplasty balloon catheter is being recalled because of the potential for the balloon not to meet burst specifications.

    Product
    Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 French sheath, 0.014" guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon le
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1745-2026·2026-04-08

    MiniMed 720G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 720G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1697-2026·2026-04-08

    da Vinci double fenestrated grasper recalled over broken grip cables

    Intuitive Surgical is recalling da Vinci S and Si Double Fenestrated Grasper Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including bl
    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-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
  • 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-1700-2026·2026-04-08

    da Vinci tenaculum forceps recalled over frayed or broken pitch cables

    Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.

    Product
    Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
    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-1748-2026·2026-04-08

    Paradigm insulin pump delivery varies with pump height changes

    Medtronic is recalling Paradigm insulin pumps models MMT-712 and MMT-715 because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    Paradigm Insulin Pump (MMT-712, MMT-715)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1661-2026·2026-04-08

    Philips Allura Xper FD10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1746-2026·2026-04-08

    MiniMed 740G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 740G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1699-2026·2026-04-08

    da Vinci grasping retractor instruments recalled over broken grip cables

    Intuitive Surgical is recalling da Vinci S and Si Grasping Retractor Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1657-2026·2026-04-08

    Atellica hemoglobin A1c assay may return depressed patient results

    Siemens is recalling Atellica CH Enzymatic Hemoglobin A1c because results may be depressed when the RCRP reagent is processed on the same analyzer, with bias increasing over time.

    Product
    Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1679-2026·2026-04-08

    Philips Azurion 5 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 5 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 5 M12; System Code: (1)722227, (2)722231;
    Category
    Medical Device
    Distribution
    Distributed nationwide