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.

44776–44800 of 50512

  • HighNHTSA·12V513000·2012-10-19

    Eldorado Buses Recalled for Defective Emergency Window Handles

    Eldorado National is recalling 2011 Axess and E-Z Rider II Max buses because emergency egress window handles may break, potentially trapping passengers.

    Product
    ELDORADO — ELDORADO AXESS, E-Z RIDER II MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13014·2012-10-18

    Dream On Me Recalls Happy Swing II Infant Swings Due to Strangulation Hazard

    Dream On Me is recalling Happy Swing II infant swings because the opening between the tray or grab bar and the seat can allow a child's body to pass through, posing a strangulation hazard.

    Product
    Happy Swing II infant swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13013·2012-10-18

    Dream On Me Recalls Bistro High Chairs Due to Strangulation Hazard

    Dream On Me is recalling Bistro high chairs because openings in the seat and tray can allow a child's neck to become entrapped, posing a strangulation risk.

    Product
    Bistro high chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0054-2013·2012-10-17

    Kardium Recalls TORQ Sternal Closure Devices Due to Metal Part Risk

    Kardium is recalling 480 units of the TORQ Sternal Closure Device because a metal part may dislodge during use.

    Product
    TORQ Sternal Closure Device. The common name is TWISTER, WIRE. The model number is TQ01A. The Catalog numbers are: 17-00001: TORQ Sternal Closure Device Shipping Carton (6-10 packs), Sterile and, 15-00001 (or 17-00002): TORQ Sternal Closure Device 10-pack - Sterile.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0022-2013·2012-10-17

    3M Recalls Steri-Vac Gas Sterilizers Due to Electrical Grounding Defect

    3M is recalling Steri-Vac 5XL and 8XL gas sterilizers because the electrical grounding mechanism did not meet safety standards.

    Product
    3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac Gas Sterilizer/Aerator is a compact unit designed to sterilize heat- and/or moisture-sensitive devices. This gas sterilizer/aerator is intended for indoor use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0077-2013·2012-10-17

    Springside Cheese Recalls White Cheddar Due to Potential Giardia Contamination

    Springside Cheese Corp is voluntarily recalling rBGH Free White Cheddar produced in late August and early September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, rBGH Free White Cheddar, 55-0172, V32 August 22, 2012.
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·12V515000·2012-10-17

    New Flyer Recalls 2010 Transit Buses Due to Weak Emergency Window Handles

    New Flyer is recalling 2010 GE35LFR and GE40LFR transit buses because emergency egress window handles may break before releasing the latch, potentially trapping passengers.

    Product
    NEW FLYER — NEW FLYER GE40LFR, GE35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0058-2013·2012-10-17

    Springside Cheese Recalls Cheddar and Horseradish Varieties Due to Giardia Risk

    Springside Cheese Corp is voluntarily recalling specific cheddar and horseradish cheeses produced in late August and early September 2012 due to potential Giardia contamination.

    Product
    Springside Cheese, Color Cheddar Horseradish Cheese, 55-0172, V2, August 24, 2012,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0071-2013·2012-10-17

    Springside Cheese Recalls Colby Cheese Due to Potential Giardia Contamination

    Springside Cheese Corp is voluntarily recalling Colby cheese produced in late August and early September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Colby Cheese, 55-0172, V3, August 27, 2012.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0063-2013·2012-10-17

    Springside Monterey Jack Dill Cheese Recalled for Giardia Contamination Risk

    Springside Cheese Corp is voluntarily recalling Monterey Jack Dill Cheese produced in August and September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Monterey Jack Dill Cheese, 55-0172, V3, August 21, 2012,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0023-2013·2012-10-17

    BioMérieux PREVI Isola System Recall for False Negative Results

    BioMérieux is recalling PREVI Isola Systems because they may fail to dispense specimens, leading to false negative microbiological test results.

    Product
    PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0032-2013·2012-10-17

    Winco Recalls Caremor Cliner Patient Recliners Due to Frame Defect

    Winco Mfg. is recalling Caremor Cliner patient recliners because a back frame may not snap properly onto the chair frame.

    Product
    Caremor Cliner is labeled in part: "***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 535 Serial No. 535A-104522***" Literature: "***Caremor Cliner 5351/5361***Winco***ISO 9001-2008 Certified***Our most comfortable and versatile recliner***Ease of…
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0046-2013·2012-10-17

    Beckman Coulter Recalls Access Folate Calibrators Due to Falsely Elevated Results

    Beckman Coulter is recalling Access Folate Calibrators because they may produce falsely elevated results that could mask a folate deficiency.

    Product
    Access Folate Calibrators, Part Number: A14207. The Access Folate assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of folic acid levels in human serum, plasma (heparin) or red blood cells using the Access Immunoassay Systems.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0025-2013·2012-10-17

    Advanced Neuromodulation Systems Recalls Eon Mini Implantable Pulse Generators

    Advanced Neuromodulation Systems is recalling 56 Eon Mini Implantable Pulse Generators manufactured in April 2012 due to a potential internal battery contact issue that could cause painful stimulation surges.

    Product
    The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel, rechargeable, multi-program system that allows the connection of one or two leads with four, eight, and 16 electrode leads. It is powered by a hermetically sealed battery within a titanium case. It uses…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0059-2013·2012-10-17

    Springside Cheese Recalls Cheddar for Potential Giardia Contamination

    Springside Cheese Corp is voluntarily recalling Color Cheddar Tomato Basil cheese produced in August and September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Color Cheddar Tomato Basil , 55-0172, V1, August 21, 2012,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0053-2013·2012-10-17

    Dae Han Tofu Soya Select Stir Fried Tofu Recalled for Labeling Error

    Pacific Northwest Tofu, LLC is recalling Dae Han Tofu Soya Select Stir Fried Tofu because soy was partially declared on the label due to a printing error.

    Product
    Stir Fried Tofu is packaged in a retail vacuum plastic package and each has net wt. 7.5 oz.. The product is sold under the Dae Han Tofu Soya Select brand. Stir Fried Tofu has the UPC 0 31499 003283.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0038-2013·2012-10-17

    Medtronic Premier Anterior Cervical Plate Screw Block Recall

    Medtronic is recalling 247 units of the Premier Anterior Cervical Plate System Screw Block because gauge lines may be misaligned, potentially causing screws to be measured as 1 mm shorter than their actual length.

    Product
    PREMIER(R) Anterior Cervical Plate System SCREW BLOCK, REF 1860503, QTY: 1 EA, Rx only, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132. Orthopedic. This instrument is a precision device which may incorporate a measuring function and has…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0075-2013·2012-10-17

    Springside Cheese Recalls Monterey Jack Roasted Red Pepper Cheese Due to Giardia Risk

    Springside Cheese Corp is voluntarily recalling Monterey Jack Roasted Red Pepper Cheese produced in late August and early September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Monterey Jack Roasted Red Pepper Cheese, 55-0172, V3, August 28, 2012.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0076-2013·2012-10-17

    Springside Monterey Jack Salsa Cheese Recalled for Potential Giardia Contamination

    Springside Cheese Corp is voluntarily recalling Monterey Jack Salsa Cheese produced in late August and early September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Monterey Jack Salsa Cheese, 55-0172, V3, August 28, 2012.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0068-2013·2012-10-17

    Springside Cheese Recalls White Cheddar Midgets Due to Giardia Risk

    Springside Cheese Corp is voluntarily recalling specific White Cheddar Midgets produced in late August and early September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Black & Green Olive White Cheddar Midget, 55-0172, V3, August 22, 2012.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0057-2013·2012-10-17

    Springside Cheese Recalls Cheddar for Potential Giardia Contamination

    Springside Cheese Corp is voluntarily recalling Blue Cheese Color Cheddar produced in August and September 2012 due to potential Giardia contamination from an employee illness.

    Product
    Springside Cheese, Blue Cheese Color Cheddar, 55-0172, V2, August 24, 2012,
    Category
    Food
    Distribution
    2 states