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.

39726–39750 of 50506

  • HighFDA (Devices)·Z-0911-2015·2015-01-14

    Siemens Symbia S Series Medical Imaging Systems Recalled for Detector Motion

    Siemens is recalling 877 Symbia S series imaging systems due to reports of unintended detector motion that may cause patient compression injuries.

    Product
    The Siemens Symbia S series is intended for use by appropriately trained health care professionals to aid in detecting, localizing, diagnosing, staging and restaging of lesions, tumors, disease and organ function for the evaluation of diseases and disorders such as, but not…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0912-2015·2015-01-14

    Siemens Symbia T Series SPECT/CT Systems Recalled for Detector Motion

    Siemens Medical Solutions USA is recalling 1,330 Symbia T series SPECT/CT systems worldwide due to reports of unintended radial detector motion that may cause patient compression injuries.

    Product
    The Siemens Symbia T series is intended for use by appropriately trained health care professionals to aid in detecting, localizing, diagnosing, staging and restaging of lesions, tumors, disease and organ function for the evaluation of diseases and disorders such as, but not…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0763-2015·2015-01-14

    Citizen Chef Organic Superfood Salad Recalled for Undeclared Milk

    Taylor Farms Pacific is recalling Citizen Chef Organic Superfood Salad due to undeclared milk on individual units. The outer packaging is labeled correctly.

    Product
    Citizen Chef Organic Superfood Salad- 4 Organic Salads. Power Greens, Walnuts, Feta, Dried Cranberries and Blueberries with Pomegranate Vinaigrette. Net Wt. 4.5 oz. (142g) USDA Organic UPC 30233 20009 Taylor Farms Pacific Stockton, CA. 95376
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0945-2015·2015-01-14

    Centurion Pacemaker Tray Recalled Due to Human Hair Contamination

    Centurion Medical Products is recalling 8 pacemaker trays because a customer reported human hair embedded in the stopper of a single unit.

    Product
    Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0940-2015·2015-01-14

    Intuitive Surgical Recalls da Vinci Si Vision Side Carts Due to Wheel Loosening

    Intuitive Surgical is voluntarily correcting 202 da Vinci Si Vision Side Carts where caster wheel bolts may unthread, causing wheels to loosen.

    Product
    IS3000 Vision Side Cart (VSC) used in conjunction with the da Vinci Si Surgical System IS3000. Product number 371683-05/Model Number VS3000 The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0925-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Remote Controls for Unintended Movement

    Trumpf Medical Systems is recalling JUPITER remote controls used with operating tables due to reports of unintended movement during surgical cases.

    Product
    (R)Cable remote control JUPITER, Material no.1219655, Serial number: to (incl.) 101998119. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer…
    Category
    Medical Device
    Distribution
    25 states
  • HighCPSC·15060·2015-01-14

    NPD Furniture Recalls Abby Dining Chairs Due to Fall Hazard

    NPD Furniture is recalling about 250 Abby Dining Chairs because the legs can break unexpectedly, posing a fall hazard. No injuries have been reported.

    Product
    Abby Dining Chair
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0927-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Operating Table Remote Controls

    Trumpf Medical Systems is recalling JUPITER operating table remote controls because damaged units may cause unintended movement during surgery.

    Product
    IR remote control JUX, Material no.1307314, Serial number: to (incl.) 102338310 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to…
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0919-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Operating Table Remote Controls

    Trumpf Medical Systems is recalling JUPITER operating table remote controls because damaged units may cause unintended movement during surgery.

    Product
    Cable remote control JUPITER / TS7500, Material no.1601926, Serial number: to (incl.) 101465919. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient…
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0928-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Operating Table Remote Controls

    Trumpf Medical Systems is recalling JUPITER operating table remote controls due to reports of unintended movement during surgical cases.

    Product
    Cable remote control JUC, BUTTON, Material no.1239823, Serial number: to (incl.) 100143048. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient…
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0902-2015·2015-01-14

    Horiba Medical Recalls ABX PENTRA Reagent Containers for Fit Issues

    Horiba Medical is recalling ABX PENTRA Reagent Containers because they may not sit properly in the rack, potentially causing incorrect test results without an alarm.

    Product
    ABX PENTRA Reagent Container, Model No. B1037307 (15 mL), B1034626 (10 mL), and B1034634 (4 mL)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0934-2015·2015-01-14

    Vision RT AlignRT 3D Imaging System Recalled for Potential Use Error

    Vision RT Inc. is recalling 55 AlignRT 3D surface imaging systems due to a potential use error when the external Gate Controller is turned on after software startup.

    Product
    AlignRT is a video-based three-dimensional (3D) surface imaging system which is used to image the skin surface of a patient in 3D before and during radiotherapy treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0913-2015·2015-01-14

    Siemens Symbia Intevo SPECT CT Systems Recalled for Detector Motion

    Siemens is recalling six Symbia Intevo SPECT CT systems worldwide because unintended detector motion may cause patient compression injuries.

    Product
    The Symbia Intevo Excel is a non-diagnostic SPECT ICT system with CT support for only attenuation correction and anatomical localization. The Symbia Intevo Series are xSPECT systems. These are SPECT and T systems integrated through xSPECT technology during image registration…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0926-2015·2015-01-14

    Trumpf Medical Systems Recalls JUPITER Operating Table Remote Controls

    Trumpf Medical Systems is recalling JUPITER operating table remote controls due to reports of unintended movement during surgical cases.

    Product
    Cable remote control JUX Material, no.1307315, Serial number: to (incl.) 101287649. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system…
    Category
    Medical Device
    Distribution
    25 states
  • HighCPSC·15059·2015-01-13

    IKEA Recalls VYSSA Crib Mattresses Due to Entrapment Hazard

    IKEA is recalling VYSSA crib mattresses because they may create gaps larger than allowed by federal regulations, posing an entrapment risk to infants.

    Product
    VYSSA crib mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V008000·2015-01-12

    Winnebago Recalls 2014-2015 Motorhomes Due to Tire Pressure Monitoring Defect

    Winnebago is recalling 2014-2015 Trend, Travato, and Itasca Viva motorhomes because the tire pressure monitoring system may fail to detect low tire pressure, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, TREND, ITASCA VIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V003000·2015-01-08

    Lance Recalls 2015 Campers and Travel Trailers Due to Awning Bracket Defect

    Lance is recalling 2015 Slide-In Campers and Travel Trailers because awning mounting brackets may crack, causing the awning to fall and potentially injure people.

    Product
    LANCE — LANCE SLIDE-IN CAMPER, TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V004000·2015-01-08

    Thor Motor Coach Recalls 2015 Motorhomes Due to Awning Screw Defect

    Thor Motor Coach is recalling 154 model year 2015 motorhomes because defective awning screws could cause the awning to fall and injure people.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR CHATEAU CITATION, PALAZZO, FOUR WINDS 5000, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender II Infusion Sets Due to Tubing Detachment

    Roche is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0762-2015·2015-01-07

    King & Prince Seafood Recalls BREADED OYSTERS Due to Norovirus

    King & Prince Seafood is recalling MRS FRIDAY'S GOURMET BREADED MEDIUM OYSTERS because the product tested positive for Norovirus GI GII.

    Product
    MRS FRIDAY'S GOURMET BREADED MEDIUM OYSTERS 18/25 CT/LB, Net Wt. 2.5 lbs (1.13 kg), Ready to Fry, Distributed by: King and Prince Seafood Corporation, Brunswick, GA 31621
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0899-2015·2015-01-07

    Smiths Medical Recalls Hypodermic Needles Due to Safety Sheath Failure

    Smiths Medical ASD, Inc. is recalling 10,000 units of Needle Pro Edge Safety Hypodermic Needles because the needle may not be captured in the safety sheath.

    Product
    Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0886-2015·2015-01-07

    Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk

    Roche Diagnostics is recalling 13,041 boxes of ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.

    Product
    ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
    Category
    Medical Device
    Distribution
    Distributed nationwide