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.

42476–42500 of 50511

  • HighNHTSA·13V600000·2013-11-25

    Haulmark Travel Trailer Recall for Door Lock Jamming Risk

    Haulmark is recalling 2006-2013 travel trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.

    Product
    HAULMARK — HAULMARK TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V599000·2013-11-25

    Wells Cargo Trailer Recall for Door Lock Jamming Risk

    Wells Industries is recalling 2006-2013 Wells Cargo trailers equipped with Fastec door locks because the deadbolt may jam, potentially trapping occupants inside.

    Product
    WELLS CARGO — WELLS CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V593000·2013-11-25

    Peterbilt Trucks Recalled for Missing Certification Label Information

    PACCAR is recalling 2004-2013 Peterbilt trucks because missing certification label information may lead to axle overloading or improper tire installation, increasing crash risk.

    Product
    PETERBILT — PETERBILT 385, 389, 386, 388
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V585000·2013-11-22

    Jayco, Starcraft, and Entegra Towable Trailer Door Lock Recall

    Jayco is recalling 2006-2014 towable trailers equipped with Fastec door locks because the key can jam the deadbolt, potentially trapping occupants inside.

    Product
    JAYCO — JAYCO, STARCRAFT, ENTEGRA TOWABLE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V591000·2013-11-22

    Volvo Bus 9700 Recalled for Insufficient Emergency Exit Windows

    Volvo is recalling 10 wheelchair-accessible 2009-2010 9700 motor coaches that lack required emergency exit windows, posing an injury risk during emergencies.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V569000·2013-11-22

    Volkswagen Recalls 2009-2011 Tiguan Vehicles for Melted Fuse Holder

    Volkswagen is recalling 2009-2011 Tiguan vehicles because a fuse holder may melt, causing partial loss of exterior lights and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14027·2013-11-21

    ElliptiGO Recalls Outdoor Elliptical Cycles Due to Fall Hazard

    ElliptiGO is recalling about 7,200 outdoor elliptical cycles in the U.S. and Canada because the front fork or drive arm axles can detach, posing a fall hazard.

    Product
    ElliptiGO outdoor elliptical cycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V586000·2013-11-21

    Carry-On Enclosed Cargo Trailer Recall for Door Lock Jamming Risk

    Carry-On is recalling 2006-2013 enclosed cargo trailers with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    CARRY-ON — CARRY-ON ENCLOSED CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V590000·2013-11-21

    Collins Recalls 2013 School Buses Due to Seat Belt Buckle Defect

    Collins Bus Corporation is recalling 333 model year 2013 school buses because seat belt buckles may fail to release, hindering emergency egress.

    Product
    COLLINS — COLLINS, COLLINS MID BUS, COLLINS CORBEIL DE516WR, DE516, DH416WR, DH400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V587000·2013-11-21

    HL Enterprise Recalls 2011-2013 Trailers With Defective Door Locks

    HL Enterprise is recalling 716 model year 2011-2013 travel, fifth-wheel, and destination trailers equipped with Fastec-brand door locks that may jam, potentially trapping occupants inside.

    Product
    BRIDGEVIEW — BRIDGEVIEW, GEORGIAN BAY, HARBORVIEW TRAVEL/5TH/DESTINATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14029·2013-11-21

    Cuisinart Recalls 7-Cup Food Processors Due to Laceration Hazard

    Cuisinart is recalling 7-cup food processors because a loose slicing disc can break the cover, posing a laceration hazard to consumers.

    Product
    Cuisinart 7-cup food processors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0162-2014·2013-11-20

    Klaire Labs Interfase Plus Enzyme Supplement Recalled for Chloramphenicol Contamination

    ProThera, Inc. is recalling Klaire Labs Interfase Plus enzyme supplements because the enzymes may be contaminated with chloramphenicol.

    Product
    Klaire Labs Interfase Plus; Enzyme Supplement; 120 Vegetarian capsules bottles. UPC 7 09616 01228 4 Manufactured by ProThera, Inc., , Klaire Labs is a division of ProThera Reno, NV 89521 Notation: Product #6 Clean Cut Enzyme wasn't entered into RES because the…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0185-2014·2013-11-20

    Fresenius Medical Care Recalls Combiset Blood Lines for Hemodialysis

    Fresenius Medical Care is recalling 24,202 cases of Combiset Blood Lines with BVM for hemodialysis. The recall addresses a risk of blood loss if connections are not tightened correctly.

    Product
    Combiset Blood Line with BVM for Hemodialysis use Catalog Number: 03-2965-9. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0209-2014·2013-11-20

    Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Calibration Drift

    Hospira is recalling Plum A+ Infusion Pumps because pressure sensor calibration drift may cause false occlusion alarms or missed occlusions.

    Product
    *** 1) Plum A+ Infusion Pump; List Number: 20678; Labeled in part: PLUM A+3; for use with Hospira MedNet; *** 2) Plum A+ Infusion Pump; List Number: 20679; Labeled in part: PLUM A+; for use with Hospira MedNet; *** 3) Plum A+ Infusion Pump with Hospira MedNet…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0231-2014·2013-11-20

    Carestream Vue PACS Software Recall for Image Loading Issues

    Carestream Health is recalling Vue PACS software because specific multi-slice images may fail to load in the viewer application.

    Product
    Carestream Vue PACS; MX-O SA WORKSTATION SW LICENSE The CARESTREAM PACS is an image management system whose intended use is to provide completely scaleable local and wide area PACS solutions for hospital and related institutions/sites, which will archive, distribute, retrieve…
    Category
    Medical Device
    Distribution
    26 states
  • HighNHTSA·13V579000·2013-11-20

    Blue Bird Recalls 2014-2015 School Buses for Seat Belt Defect

    Blue Bird is recalling 2014-2015 Vision and All American school buses because the driver's seat belt latch may fail to release, hindering emergency egress.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0143-2014·2013-11-20

    Apex Energetics Recalls Four Supplements Due to Chloramphenicol Contamination

    Apex Energetics is recalling four dietary supplements because they may contain trace amounts of the antibiotic chloramphenicol from a raw material supplier.

    Product
    LGS-Zyme (Z12), Enzyme-Based Multivitamin & Amino Acid Dietary Supplement, 120 Capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0150-2014·2013-11-20

    Empirical Labs Recalls Tri-Mins Dietary Supplements Due to Chloramphenicol

    Empirical Labs is recalling specific lots of Tri-Mins Daily Foundation dietary supplements because they may be contaminated with chloramphenicol.

    Product
    Dynamite Specialty Products Tri-Mins Daily Foundation, calcium, magnesium, potassium dietary supplement; 240 Capsules; Manufactured for Dynamite Marketing, Inc, Meridian, ID 83642.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0242-2014·2013-11-20

    Carestream Vue PACS Software Recall for Image Loading Issues

    Carestream Health is recalling Vue PACS software because specific multi-slice images may fail to load in the viewer application.

    Product
    Carestream Vue PACS; UPG MX-O SVR 25K EX/YR UNLIMITED The CARESTREAM PACS is an image management system whose intended use is to provide completely scaleable local and wide area PACS solutions for hospital and related institutions/sites, which will archive, distribute, retrieve…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-0168-2014·2013-11-20

    Oh Bok Bakery Recalls Walnut Cookies for Undeclared Wheat Flour

    Cho & So, Inc. is recalling walnut-shaped soft cookies because wheat flour was not declared on the label, posing a risk to individuals with wheat allergies.

    Product
    Walnut shaped soft Cookie packed on styrofoam tray with plastic over wrap ASSI brand Korean Cake 20644D Net Wt.: 8 oz. Distributed by Rhee Bros., Inc. 7461 Coca Cola Dr Hanover, MD 21076 Expiration date 3/20/14 With Korean language labeling
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0184-2014·2013-11-20

    Fresenius Hemodialysis Blood Lines Recalled for Potential Disconnection Risk

    Fresenius Medical Care is recalling 8,528 cases of 2008K@ Home Blood lines due to a risk of disconnection and blood loss if not tightened correctly.

    Product
    2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis use Catalog Number: 03-2962-3. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0201-2014·2013-11-20

    Toshiba Titan 3T MRI System Recalled for SAR Display Error

    Toshiba is recalling 18 Titan 3T MRI systems because they may display lower Specific Absorption Rate (SAR) values than actual when used with specific coils.

    Product
    Titan 3T MRI System, MRT-3010A/5. Product Usage: Usage: MRI system.
    Category
    Medical Device
    Distribution
    Distributed nationwide