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.

41201–41225 of 50511

  • HighFDA (Devices)·Z-1604-2014·2014-05-21

    Zimmer Cartilage Knee Brace Recalled Due to Latex Contamination

    Zimmer, Inc. is recalling 2,222 units of Cartilage Knee Braces because raw material labeled as latex-free actually contained latex.

    Product
    Cartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment and support of many types of knee injuries or following surgical and nonsurgical correction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1613-2014·2014-05-21

    Siemens Syngo Dynamics PACS Recalled for Patient Demographics Display Error

    Siemens Medical Solutions is recalling 50 Syngo Dynamics v9.5 systems due to a software error that may cause incorrect patient demographics to be displayed.

    Product
    Syngo Dynamics v9.5 system. A Picture Archiving and Communication System (PACS) intended for acceptance, transfer, display, storage, archive and manipulation of digital medical images, including quantification and report generation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1575-2014·2014-05-21

    Blue Belt Technologies Recalls Navio PFS Orthopedic Sterotaxic Instrument

    Blue Belt Technologies is voluntarily recalling 11 Navio PFS systems used in orthopedic knee surgery due to a potential electronic module defect that could cause latent failure.

    Product
    NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1607-2014·2014-05-21

    HeartWare HVAD Pump Implant Kit Battery Recall for Support Issues

    HeartWare Inc is recalling HVAD Pump Implant Kit batteries that may not provide two hours of support or behave unusually.

    Product
    HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage ventricular heart failure.The HeartWare VAS is designed for in-hospital and…
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Food)·F-1938-2014·2014-05-21

    Fong Kee Tofu Soy Bean Cake Recalled for Undeclared Wheat Allergen

    Fong Kee Tofu Co., Inc. is recalling Soy Bean Cake products because they contain wheat, a sub-ingredient of soy sauce, that is not declared on the label.

    Product
    Soy Bean Cake Net Wt. 9. oz. Ingredient: Soybeans, water, salt, Soy sauce, Spice, Calcium Sulfate. Perishable, keep refrigerated. Fong Kee Tofu Inc. 1135 Revere Ave. San Francisco, CA 94124.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1620-2014·2014-05-21

    Baxter Recalls RAPIDFILL Syringe Strips Due to Sterile Barrier Breach

    Baxter Corporation is recalling RAPIDFILL Syringe Strips because of a possible breach in the sterile barrier of the inner and outer bags.

    Product
    RAPIDFILL Syringe Strip, For use with RAPIDFILL Automated Syringe Filler (ASF): H93890200 RAPIDFILL Syringe Strip, White. H93890221 RAPIDFILL Syringe Strip, Yellow. H93890222 RAPIDFILL Syringe Strip, Orange. H93890223 RAPIDFILL Syringe Strip, Red. H93890225 RAPIDFILL Syringe…
    Category
    Medical Device
    Distribution
    21 states
  • HighNHTSA·14V268000·2014-05-21

    Stoughton Trailers Recall 2014 Models for Suspension Pivot Bolt Failure

    Stoughton is recalling 879 specific 2014 trailers because suspension pivot bolts may fail, potentially causing the axle to separate and increasing crash risk.

    Product
    STOUGHTON — STOUGHTON AVW, ZGPVW, AHV, AVXW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V269000·2014-05-21

    Eldorado Aerotech 240 Recalled for Wheelchair Lift Cable Fire Risk

    Eldorado is recalling 2012-2014 Aerotech 240 vehicles because a wheelchair lift cable may not clear the lift, potentially causing a short circuit and fire.

    Product
    ELDORADO — ELDORADO AEROTECH 240
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1618-2014·2014-05-21

    Fresenius Hemodialysis Machines Recalled for Potential UF Pump Detection Failure

    Fresenius Medical Care is recalling 79 hemodialysis machines and replacement parts because they may fail to detect a disconnected Ultrafiltration (UF) Pump.

    Product
    Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards and also sold as replacement parts for use with Fresenius 2008-Series Hemodialysis Machines (2008K, 2008K2, 2008K@home and 2008T). Part Number: 190234 Revision K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1621-2014·2014-05-21

    InterValve V8 Balloon Aortic Valvuloplasty Catheter Recalled for Leak Issues

    InterValve Inc is recalling specific V8 Balloon Aortic Valvuloplasty Catheters due to leak issues discovered during accelerated age testing.

    Product
    InterValve V8 Balloon Aortic Valvuloplasty Catheter, model 172212C110, 192412C110, 212612C110, 232812C110. Used in Cardiovascular procedures for Balloon Aortic Valvuloplasty.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1603-2014·2014-05-21

    Zimmer Drop Lok Knee Brace Recalled Due to Latex Contamination

    Zimmer, Inc. is recalling Drop Lok Knee Braces because raw material labeled as latex-free was found to contain latex. The recall affects 131 units distributed in the US and internationally.

    Product
    DROP LOK" Knee Brace***LATEX FREE" Product Usage: Used in the treatment, support, and rehabilitation of many types of knee injuries or following surgical correction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V266000·2014-05-20

    GM Recalls 2009-2014 SUVs for Seatbelt Cable Defect

    General Motors is recalling specific 2009-2014 Buick, Chevrolet, GMC, and Saturn SUVs because a seatbelt cable may separate, increasing injury risk in a crash.

    Product
    BUICK — BUICK, GMC, SATURN ENCLAVE, ACADIA, OUTLOOK, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E025000·2014-05-19

    Agility Fuel Systems Recalls CNG Fuel Tank Systems for Valve Defect

    Agility Fuel Systems is recalling CNG Fuel Tank Systems where the manual shutoff valve may get stuck closed, posing a safety risk to service personnel.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V259000·2014-05-16

    GM Recalls 2015 Cadillac Escalade Models for Air Bag Defect

    General Motors is recalling 2,838 2015 Cadillac Escalade and Escalade ESV vehicles because the front passenger air bag may only partially deploy in a crash.

    Product
    CADILLAC — CADILLAC ESCALADE, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E023000·2014-05-16

    Harley-Davidson Recalls 2014 XL Sportster Brake Lever Kits

    Harley-Davidson is recalling accessory brake lever kits for 2014 XL Sportster motorcycles because excess chrome plating may prevent the front brake from releasing, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XL SPORTSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V263000·2014-05-16

    Nissan Recalls 2014 LEAF Vehicles Due to Inverter Failure Risk

    Nissan is recalling 2014 LEAF vehicles because a motor control circuit board defect may cause the inverter to fail, leading to an unexpected vehicle shut down.

    Product
    NISSAN — NISSAN LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V253000·2014-05-15

    GM Recalls 2014 Cadillac CTS for Windshield Wiper Failure Risk

    General Motors is recalling 2014 Cadillac CTS vehicles because the windshield wipers may stop working after a jump start, increasing crash risk.

    Product
    CADILLAC — CADILLAC CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14182·2014-05-15

    StyleCraft Recalls Upholstered Benches Due to Fall Hazard

    StyleCraft is recalling upholstered benches sold at HomeGoods because they can crack and break, posing a fall hazard. No injuries have been reported.

    Product
    Upholstered Benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14180·2014-05-15

    H&M Recalls Girls' Leggings Due to Choking Hazard

    H&M is recalling approximately 65,000 girls' leggings because a metal part on the belt can detach, posing a choking hazard to young children.

    Product
    Girls' Leggings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14183·2014-05-15

    BMC Recalls Three Bicycle Models Due to Fork Breakage Hazard

    BMC is recalling approximately 160 Alpenchallenge, Masschallenge, and Urbanchallenge bicycles because the carbon forks can crack or break, posing a fall hazard.

    Product
    BMC Alpenchallenge, Masschallenge and Urbanchallenge Bicycles with Aprebic Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1922-2014·2014-05-14

    Bread Stop Bakery Recalls Flaxseed Bread Due to Undeclared Soy Allergen

    Bread Stop Bakery is recalling 80 loaves of Flaxseed Bread because an anti-stick spray containing soy lecithin was used during manufacturing, but soy was not declared on the label.

    Product
    the BREAD STOP Flaxseed Bread 24 oz. The bread is packaged in a plastic bag and twist tie, with the label inside the bag.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1553-2014·2014-05-14

    Siemens ADVIA Centaur XP Immunoassay System Recalled for Gas Spring Failure

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur XP Immunoassay systems because gas springs may fail, causing the instrument cover to fall.

    Product
    ADVIA Centaur XP Immunoassay system, an automated in vitro diagnostic analyzer. Catalog # 078-A011-03 - ADVIA Centaur XP, Catalog # 078-A011R03 - ADVIA Centaur XP refurb.
    Category
    Medical Device
    Distribution
    Distributed nationwide