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.

40476–40500 of 50511

  • HighNHTSA·14E063000·2014-09-22

    Auto Pro Recalls Steering Hub Adapters for 1969-1970 Camaros

    Auto Pro USA is recalling aftermarket steering hub adapters for 1969 and 1970 Camaros because they may cause the steering wheel to become misaligned, increasing the risk of a crash.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V578000·2014-09-22

    Starcraft RV Recalls 2015 AR-One Travel Trailers for Fire Risk

    Starcraft RV is recalling 72 model year 2015 AR-One travel trailers because inadequate kitchen venting could allow propane gas to ignite, causing a fire.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E064000·2014-09-22

    Auto Pro Recalls Steering Hub Adapters for 1967-1968 Camaros

    Auto Pro USA is recalling steering hub adapters for 1967 and 1968 Camaros because they may cause the steering wheel to misalign, increasing crash risk.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V572000·2014-09-19

    Navistar Recalls 2015 International Durastar and IC Bus CE Vehicles

    Navistar is recalling 2015 International Durastar and IC Bus CE vehicles because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.

    Product
    IC BUS — IC BUS, INTERNATIONAL CE, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14278·2014-09-18

    Siemens Recalls SBGA-34 Audible Fire Alarm Bases Due to Injury Risk

    Siemens is recalling about 9,000 SBGA-34 audible fire alarm bases because they may fail to sound an alarm, posing a risk of personal injury and property damage.

    Product
    SBGA-34 Audible Fire Alarm Base
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2433-2014·2014-09-17

    Laura Lynn French Onion Dip Recalled for Undeclared Wheat

    Durrset Amigos, Ltd. is recalling Laura Lynn French Onion Dip due to undeclared wheat. The product was distributed in Texas, Wisconsin, and North Carolina.

    Product
    Laura Lynn French Onion; DIP; NET WT 9 OZ (255g); DISTRIBUTED BY INGLES MARKETS, INC.; ASHEVILLE, NC 28816. Shipped in cases of 12.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2617-2014·2014-09-17

    GE Healthcare Recalls CARESCAPE Respiratory Modules Due to O2 Sensor Failure

    GE Healthcare is recalling 748 CARESCAPE respiratory modules and Airway Gas Options due to a potential O2 sensor component failure.

    Product
    CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE; the Airway Gas Option N-CAiO and respective service exchange units. The affected modules could be in use with any of the following GE host devices: -CARESCAPE respiratory modules with…
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Devices)·Z-2609-2014·2014-09-17

    Ab Sciex API 3200MD System Recalled for Incorrect Diagnostic Data

    Ab Sciex is recalling six API 3200MD LC/MS/MS systems because the MultiQuant 3.0 software may provide incorrect data for patient diagnosis.

    Product
    AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens Part Number 5024543.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-2431-2014·2014-09-17

    Roundy's Salsa Con Queso Recalled for Undeclared Wheat

    Durrset Amigos, Ltd. is recalling Roundy's Salsa Con Queso because a supplier used wheat instead of whey in the cheese premix, creating an undeclared wheat allergen.

    Product
    Roundy's Salsa Con Queso; NET WT; 16 OZ (1 LB) 454g; DISTRIBUTED BY Roundy's Milwakee, WI 53202. Distributed in cases of 12/16 W jars.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2614-2014·2014-09-17

    Baxter Recalls Buretrol Solution Sets Due to Chamber Separation

    Baxter Healthcare is voluntarily recalling specific lots of Buretrol Solution Sets because the burette chamber may separate from the drip chamber.

    Product
    ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip Chamber Filter Valve***3 Luer Activated Valves***Male Luer Lock Adapter***with Retractable Collar***Fluid path is Sterile, Nonpyrogenic. ****Indications for Use: For the administration of fluids from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2429-2014·2014-09-17

    H-E-B Chipotle Con Queso Recalled for Undeclared Wheat

    Durrset Amigos, Ltd. is recalling H-E-B Chipotle Con Queso because a supplier used wheat instead of whey in the cheese premix, creating an undeclared wheat allergen.

    Product
    H-E-B Chipotle Con Queso; HOT; with Real Chipotle Peppers; NET WT; 16 OZ (1 LB) 454g; Made with Pride and Care for H-E-B, SAN ANTONIO, TEXAS 78204. Distributed in cases of 12/16 oz. jars.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2428-2014·2014-09-17

    Marjon Spicy Sprouts Recalled Due to Listeria Contamination

    Marjon Specialty Foods is recalling Marjon Spicy Sprouts because environmental samples found Listeria in the production area.

    Product
    Marjon Spicy Sprouts, NET WT. 6/6 oz. packaged in bags; Marjon Specialty Foods, Inc. 3508 Sydney Rd., Plant City, FL 33567 Grown and Packed in the USA. UPC 010077554000197. Used by 7/06/14.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2611-2014·2014-09-17

    Illumina Worklist Manager Software Recalled for Performance Failure

    Illumina Inc is recalling 35 units of Illumina Worklist Manager software v1.0.15 because it fails to perform as intended.

    Product
    Illumina Worklist Manager (IWM) (software v1.0.15), a component of Illumina MiSeqDx Platform. Product Usage: The Illumina MiSeqDx is a sequencing instrument that measures fluorescence signals of labeled nucleotides through the use of instrument specific reagents and flow…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2420-2014·2014-09-17

    CT Concerns Recalls Fresh Wild Tuna and Salmon for Listeria Risk

    CT Concerns, Inc. is voluntarily recalling fresh wild tuna and farmed Atlantic salmon due to potential Listeria monocytogenes contamination found in environmental swabs.

    Product
    Fresh Wild Tuna. No finished packaging. Fresh Tuna is placed in white styrofoam box and delivered to area restaurants.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2601-2014·2014-09-17

    Wright Medical Recalls CLAW II 2 Hole Plate OrthoLoc 3DSi Orthopedic Plates

    Wright Medical Technology is recalling 497 CLAW II 2 Hole Plate OrthoLoc 3DSi orthopedic plates because they were manufactured from an incorrect raw material.

    Product
    CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 15mm, REF 40240215, 1 EACH, Rx ONLY, NON STERILE Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2605-2014·2014-09-17

    Wright Medical Recalls CLAW II Straight Plate OrthoLoc 3DSi Orthopedic Devices

    Wright Medical Technology is recalling 66 units of CLAW II Straight Plate OrthoLoc 3DSi orthopedic devices because they were manufactured from an incorrect raw material.

    Product
    CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 20mm, REF 40242020, 1 EACH, Rx ONLY, NON STERILE Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2603-2014·2014-09-17

    Wright Medical Recalls CLAW II Orthopedic Plates Due to Incorrect Material

    Wright Medical Technology is recalling 400 CLAW II 2 Hole Plate Ortholoc 3DSi units because they were manufactured from an incorrect raw material.

    Product
    CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 25mm, REF 40240225, 1 EACH, Rx ONLY, NON STERILE Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2419-2014·2014-09-17

    CT Concerns Recalls Fresh Salmon and Tuna for Listeria Risk

    CT Concerns, Inc. is voluntarily recalling fresh Atlantic salmon and wild tuna due to potential Listeria monocytogenes contamination detected in environmental swabs.

    Product
    Fresh Atlantic Salmon. No finished packaging. Fresh Salmon is placed in white styrofoam box and delivered to area restaurants.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2610-2014·2014-09-17

    Ethicon Recalls PROXIMATE Skin Staplers Due to Unformed Staple Risk

    Ethicon Endo-Surgery Inc is recalling PROXIMATE skin staplers because a non-conforming component may cause the device to fire an unformed staple.

    Product
    PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler (Model PXR35), Bulk/Non-Sterile PROXIMATE RH Rotating-Head Skin Stapler (Model CK 117), and Bulk/Non-Sterile PROXIMATE PX Fixed-Head Skin Stapler (Model CK…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2426-2014·2014-09-17

    Marjon Bean Sprouts Recalled Due to Listeria Contamination in Production Area

    Marjon Specialty Foods is recalling bean sprouts after Listeria was found in environmental samples from the production area.

    Product
    Marjon Bean Sprouts, Keep Fresh Zip Lock: Keep Refrigerated. NET WT. 8/8 oz. plastic bag; 5 lb bag and 2/5 Bags; Marjon Specialty Foods, Inc. 3508 Sydney Rd., Plant City, FL 33567 Grown and Packed in the USA. UPC codes: 10077554000012; 0200077554000466; 010077554000463 Used by…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2604-2014·2014-09-17

    Wright Medical Recalls CLAW II Orthopedic Plates Due to Incorrect Raw Material

    Wright Medical Technology is recalling 178 CLAW II 2 Hole Plate Ortholoc 3DSi units because they were manufactured from an incorrect raw material.

    Product
    CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 30mm, REF 40240230, 1 EACH, Rx ONLY, NON STERILE Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2616-2014·2014-09-17

    Pioneer Surgical Technology Recalls Streamline MIS Spinal Fixation System Fixed Rod Holders

    Pioneer Surgical Technology is recalling nine Streamline MIS Spinal Fixation System Fixed Rod Holders because they failed to lock onto the spinal rod.

    Product
    Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE, Rx only The Streamline MIS Spinal Fixation System is intended for posterior, noncervical pedicle fixation, T1-S2. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2599-2014·2014-09-17

    Wright Medical Recalls Orthopedic Claw Plates Due to Incorrect Raw Material

    Wright Medical Technology is recalling specific orthopedic claw plates because they were manufactured from an incorrect raw material.

    Product
    CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM, REF 40S20020, 1 EACH, Rx ONLY, NON STERILE Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2427-2014·2014-09-17

    Marjon Kale Sprouts Recalled Due to Listeria Contamination in Production Area

    Marjon Specialty Foods is recalling Marjon Kale Sprouts because Listeria was found in environmental samples from the production area.

    Product
    Marjon Kale Sprouts, Keep Refrigerated. NET WT. 6/3 oz. packaged in cups; Marjon Specialty Foods, Inc. 3508 Sydney Rd., Plant City, FL 33567 Grown and Packed in the USA. UPC 20077554000231. Used by 7/06/14.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2430-2014·2014-09-17

    Hill Country Fare Salsa Con Queso Recalled for Undeclared Wheat

    Durrset Amigos, Ltd. is recalling Hill Country Fare Salsa Con Queso Sauce due to undeclared wheat, a common allergen.

    Product
    HILL COUNTRY FARE; Salsa Con QUESO Sauce; Medium - PICANTE; NET WT 16 OZ (1LB) CONT. NET. 454g; DISTRIBUTED BY: H-E-B, SAN ANTONIO, TX 78294. distributed in cases of 12/16 oz. jars
    Category
    Food
    Distribution
    3 states