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

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2951–2975 of 39824

  • HighFDA (Devices)·Z-0037-2026·2025-10-15

    Angiography systems recalled over collimator returning to default region of interest

    Canon Medical Systems is recalling eight radiography/fluoroscopy systems because changing the acquisition program returns the collimator to a default ROI, leaving the X-ray area partially covered by a static image.

    Product
    This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0128-2026·2025-10-15

    Nasal feeding tubes recalled because distal tips may detach too easily

    Applied Medical Technology is recalling 390 NutraGlide nasal feeding tubes whose distal tips may detach at lower than expected forces.

    Product
    NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0129-2026·2025-10-15

    Shorter 8 French feeding tubes recalled because distal tips may detach

    Applied Medical Technology is recalling 840 NutraGlide 5 F - 8 F x 55 nasal feeding tubes whose distal tips may detach at lower than expected forces.

    Product
    NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0044-2026·2025-10-15

    Radiography suites recalled because X-ray tube mounting shaft may break

    FUJIFILM is recalling 16 FDR Visionary Suite systems because the shaft mounting the X-ray tube unit on the support may break, with protective parts possibly not working.

    Product
    FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23, (2) 566-16130-31, (3) 566-16130-33
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0039-2026·2025-10-15

    Ocular surgical matrix recalled after complaints of early patch exposure

    CorNeat Vision is recalling 630 CorNeat EverPatch units after reviewed complaints identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

    Product
    CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0130-2026·2025-10-15

    Larger nasal feeding tubes recalled because distal tips may detach

    Applied Medical Technology is recalling 200 NutraGlide 5 F - 8 F nasal feeding tubes whose distal tips may detach at lower than expected forces.

    Product
    NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0127-2026·2025-10-15

    Shorter 6 French feeding tubes recalled because distal tips may detach

    Applied Medical Technology is recalling 1,780 NutraGlide 5 F - 6 F x 55 nasal feeding tubes whose distal tips may detach at lower than expected forces.

    Product
    NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0040-2026·2025-10-15

    Scleral reinforcement matrix recalled after complaints of early patch exposure

    CorNeat Vision is recalling 180 EverPatch+ units after reviewed complaints identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

    Product
    EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0107-2026·2025-10-15

    FlexLab X system recalled over unevaluated blood sample integrity function

    Inpeco is recalling one FlexLab X system because the Sample Integrity Module's hemolysis, icterus and lipemia function has not been evaluated by the FDA.

    Product
    FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0121-2026·2025-10-15

    Continuous epidural anesthesia sets recalled over catheter connector lid position

    B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Sets, product code CE17TFC, because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged, PERIFIX FX Springwound Epidural Catheter - 19 Ga. Closed tip. Product Code: CE17TFC. Product Description: CE17TFC CONTINUOUS EPID SET W/17G TUOHY.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0120-2026·2025-10-15

    Open tip epidural trays recalled over catheter connector lid position

    B. Braun is recalling 2,760 PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFS, because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Open tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFS. Product Description: CE17TKFS EPIDURAL TRAY.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0118-2026·2025-10-15

    Fixed wing epidural trays recalled over catheter connector lid position

    B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFSDT, because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Fixed Wings, 19 Ga. Open tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFSDT. Product Description: CE17TKFSDT EPID TRAY W/17GA FIXED WING.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0041-2026·2025-10-15

    High flux dialyzers recalled to instruct users on newly redesigned press-on caps

    Fresenius Medical Care is issuing a recall covering Optiflux High Flux E-beam Dialyzers to tell users that the caps changed from threaded to press-on and must be pressed firmly to affix.

    Product
    Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX F160NRe 12/CS 1.5SA EBEAM, (2) 0500318E OPTIFLUX F180NRe 12/CS 1.7SA EBEAM, (3) 0500320E OPTIFLUX F200NRe 12/CS 1.9SA EBEAM, (4) 0500325E OPTIFLUX F250NRe 12/CS 2.5SA EBEAM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0119-2026·2025-10-15

    Epidural anesthesia trays recalled over catheter connector lid position defect

    B. Braun is recalling 21,270 PERIFIX FX Continuous Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFCS. Product Description: CE17TKFCS CONT EPID TRAY W/17G TUOHY-LF.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0122-2026·2025-10-15

    ESPOCAN spinal epidural trays recalled over catheter connector lid position

    B. Braun is recalling 10,130 ESPOCAN Combined Spinal and Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.

    Product
    ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 25 Ga. x 5 in. (12.7 cm) Spinal Needle with Marking and Centering Sleeve, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: ES1725KF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0072-2026·2025-10-15

    Collagen vascular grafts recalled over incorrect labels missing CE and UKCA marks

    LeMaitre Vascular is recalling 10 Artegraft Collagen Vascular Grafts distributed with an incorrect label lacking CE and UKCA marks and without the patient leaflet and implant card.

    Product
    Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is intended to serve as a substitute conduit for blood where bypass or replacement of occluded or diseased arterial segments is required or to establish a c
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0115-2026·2025-10-15

    Epidural fixed trays recalled over catheter connector lid position defect

    B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFCPS, because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFCPS. Product Description: CE17TKFCPS EPIDURAL FULL TRAY.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0125-2026·2025-10-15

    Combined spinal epidural trays recalled over catheter connector lid position issue

    B. Braun is recalling 60 Combined Spinal and Epidural Anesthesia Tray 2 units because the lid of the catheter connector may be in the incorrect position.

    Product
    Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: SESK. Product Description: SESK COMBINED SPINAL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0071-2026·2025-10-15

    Phosphorus reagent lots recalled because calibration may fail before expiration date

    Beckman Coulter is recalling 2,146 units of SYNCHRON Systems Phosphorus reagent because specific lots may fail calibration before the lot expiration date, delaying patient results.

    Product
    SYNCHRON Systems Phosphorus (PHOSm) Reagent REF: 467868 For In Vitro Diagnostic Use, Rx Only.
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0116-2026·2025-10-15

    Winged closed tip epidural trays recalled over catheter connector lid position

    B. Braun is recalling 48,110 PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFC, because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFC. Product Description: CE17TKFC EPIDURAL TRAY W/ 17GA TUOHY.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0114-2026·2025-10-15

    Epidural basic trays recalled over catheter connector lid position defect

    B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TBFC, because the lid of the catheter connector may be in the incorrect position.

    Product
    PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and PERIFIX FX Springwound Catheter - 19 Ga. Closed Tip. Product Code: CE17TBFC. Product description: CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0123-2026·2025-10-15

    Open tip spinal epidural trays recalled over catheter connector lid position

    B. Braun is recalling 2,840 Combined Spinal and Epidural Anesthesia Trays, product code NES1727KFX, because the lid of the catheter connector may be in the incorrect position.

    Product
    Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle and 19 Ga. Open Tip PERIFIX FX Springwound Epidural Catheter. Product Code: NES1727KFX. Product Description: NES1727KFX W /17GA T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0126-2026·2025-10-15

    Custom epidural anesthesia trays recalled over catheter connector lid position

    B. Braun is recalling 5,770 Design Options PERIFIX FX Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.

    Product
    Design Options, PERIFIX FX Epidural Anesthesia Tray. Product Code: CESK. Product Descriptions: 1. CESK ROBERT WOOD JOHNSON UNIV HOSP. 2. CESK EAST JEFFERSON GEN HOSP 20071769. 3. CESK FLETCHER ALLEN HOSPITAL. 4. CESK WASHOE MEDICAL CENTER. 5. CESK DETROIT MEDI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0124-2026·2025-10-15

    Pain management trays recalled over catheter connector lid position defect

    B. Braun is recalling 2,450 Design Options Pain Management Trays because the lid of the catheter connector may be in the incorrect position.

    Product
    Design Options, Pain Management Tray. Product Code: SESK. Product Descriptions: 1. SESK PARKLAND MEMORIAL FX CSE TRAY. 2. SESK OWENSBORO DAVIESS HOSP 20058814. 3. SESK MEMORIAL HEALTH SYSTEM SPINAL/EPID. 4. SESK ST. JOHN'S MERCY MED CTR SPINAL/EPID. 5. SESK MAIMONI
    Category
    Medical Device
    Distribution
    Distributed nationwide