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.

43551–43575 of 50511

  • HighFDA (Devices)·Z-1365-2013·2013-05-29

    Medical Information Technology Recalls Bi-Directional Communication Analyzer Interface

    Medical Information Technology, Inc. is recalling 56 MEDITECH Bi-Directional interactive Communication Analyzer Interface devices due to incorrect transmission of laboratory results.

    Product
    MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1346-2013·2013-05-29

    Roche Recalls cobas 4800 Systems Due to Rare Channel Shift Errors

    Roche Molecular Systems is recalling 425 cobas 4800 systems because rare channel-shift errors may cause test results to be reported in the wrong channel.

    Product
    cobas¿ 4800 system z480 instrument. Integrates fully automated total nucleic acid isolation directly from secondary sample tubes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1415-2013·2013-05-29

    Wild Harvest Organic Cranberry Juice Recalled for Patulin Contamination

    Clement Pappas & Co. is recalling Wild Harvest Organic Cranberry Juice because an ingredient contained patulin levels between 57.4 and 100 ppb.

    Product
    wild harvest organic cranberry 64 FL OZ (2 QTS) 1.89L UPC 011535500408 Distributed by Supervalu Inc. Eden Prairie, MN 55344 USA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1419-2013·2013-05-29

    Meijier Organics Cranberry Juice Recalled for Patulin Contamination

    Clement Pappas & Co. is recalling Meijier Organics Cranberry Juice because an ingredient contained patulin levels between 57.4 and 100 ppb.

    Product
    meijier Organics Cranberry Juice Net 64 FL OZ(2 QT) 1.89 L UPC 719283661562 Dist By Meijier Distribution Inc. Grand Rapids, MI 49544
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-431-2013·2013-05-29

    Levoxyl Levothyroxine Sodium Tablets Recalled for Low Potency

    King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1418-2013·2013-05-29

    Simple Truth Organic Apple Juice Recalled for Patulin Contamination

    Clement Pappas & Co. is recalling Simple Truth Organic Apple Juice because it contains patulin levels exceeding safety limits.

    Product
    simple truth organic Apple Juice 100% 64 FL OZ (2 QT) 1.89 L UPC 011110834805 Distributed by The Kroger Co. Cincinnati OH 45202
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-424-2013·2013-05-29

    Levoxyl Tablets Recalled for Low Potency at Expiry

    King Legacy is recalling Levoxyl tablets because they were below specification for potency at the expiry stability point.

    Product
    LEVOXYL — LEVOXYL (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·13E026000·2013-05-29

    Brake Parts Inc. Recalls Hydro-Max Brake Master Cylinders for Fluid Indicator Defect

    Brake Parts Inc. is recalling specific Hydro-Max brake master cylinders because the fluid level indicator may fail to warn drivers of low brake fluid, potentially increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1361-2013·2013-05-29

    Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes

    Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because product coatings require 510K approval.

    Product
    Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Needle 2.75" (6.99cm) Length, Product number P0013 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13201·2013-05-29

    H&M Recalls Children's Water Bottles Due to Choking Hazard

    H&M is reannouncing a recall of children's water bottles because the spouts can break off, posing a choking hazard. Consumers should stop using the bottles and contact H&M for a refund.

    Product
    Children's Water Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1445-2013·2013-05-29

    Alfred Louie Inc. Recalls Soy Bean Sprouts Due to Listeria Contamination

    Alfred Louie Inc. is recalling 5-pound bags of soy bean sprouts because FDA environmental samples detected Listeria monocytogenes in the facility.

    Product
    Soy Bean Sprouts: Keep Refrigerated: Ingredients:Soy Beans Net WT: 5 lbs (2.27 KG); Alfred Louis Inc., Bakersfield, CA 93309 Product of the USA.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1355-2013·2013-05-29

    Progressive Medical Recalls PTFE Coated Laparoscopic Electrodes

    Progressive Medical is recalling PTFE coated laparoscopic electrodes because the product coatings require 510K approval.

    Product
    Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -Laparoscopic Electrode PTFE Coated Curved Blade 33cm Length, Product number P0019 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1363-2013·2013-05-29

    Progressive Medical Recalls PTFE Coated Laparoscopic Electrosurgical Electrodes

    Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.

    Product
    Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J- Hook 44cm Length, Product number P0021X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13203·2013-05-29

    KTM and Husaberg Motorcycles Recalled Due to Throttle Cable Malfunction

    KTM North America is recalling about 7,000 KTM and Husaberg motorcycles because a malfunctioning throttle cable can cause an uncontrollable throttle, posing a crash hazard.

    Product
    Competition/Closed Course and Enduro Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1353-2013·2013-05-29

    Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes

    Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because product coatings require 510K approval.

    Product
    Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 44cm Length, Product number P0020X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V222000·2013-05-28

    PACCAR Recalls 2014 Kenworth and Peterbilt Trucks for Ignition Switch Defect

    PACCAR is recalling specific 2014 Kenworth and Peterbilt trucks because an ignition switch defect can cause the engine to start unexpectedly, posing a risk of injury or crash.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T370, T660, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V221000·2013-05-28

    New Flyer Transit Buses Recalled for Defective Push-to-Start Switches

    New Flyer is recalling certain 2012-2013 transit buses because a weak spring in the push-to-start switch may allow the engine to start unexpectedly, posing an injury risk to nearby workers.

    Product
    NEW FLYER — NEW FLYER XD40, XN40, XD35, XD60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V220000·2013-05-24

    GM Recalls 9,677 Vehicles for Intermittent Brake Light Flashing

    General Motors is recalling 9,677 Cadillac and Chevrolet vehicles because brake lamps may flash without braking, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET XTS, SONIC, ATS, IMPALA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E030000·2013-05-24

    BMW Recalls Dealer-Installed Luggage Racks for 2013 C650 GT Scooters

    BMW is recalling dealer-installed luggage racks for 2013 C650 GT Maxi-Scooters because attachment bolts may loosen, causing the rack to separate and create a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide