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.

26451–26475 of 50460

  • HighFDA (Food)·F-0987-2019·2019-02-27

    Sysco Recalls Harbor Seafood Crab Meat Due to Temperature Failure

    Sysco Charlotte is recalling Harbor Seafood Crab Meat Backfin Past Asia because a cooler malfunction caused the product to be held at unsafe temperatures.

    Product
    Harbor Seafood CRAB MEAT BACKFIN PAST ASIA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0941-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Due to Salmonella Risk

    Ardent Mills is voluntarily recalling certain lots of Westcreek Self-Rising Flour because they may be contaminated with Salmonella.

    Product
    WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0998-2019·2019-02-27

    Sysco Recalls Sea Wings Crab Meat Special Due to Temperature Failure

    Sysco Charlotte is recalling Sea Wings CRAB MEAT SPECIAL PAST ASIA because a cooler malfunction meant the food was not held at appropriate temperatures, potentially making it unsafe.

    Product
    Sea Wings CRAB MEAT SPECIAL PAST ASIA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0507-2019·2019-02-27

    Dr. Reddy's Recalls Divalproex Sodium Tablets for Dissolution Failure

    Dr. Reddy's is recalling 10,656 bottles of Divalproex Sodium Extended-release Tablets because they failed to meet dissolution specifications.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1048-2019·2019-02-27

    Katy's Kitchen Roasted Sunflower Kernels Recalled for E. coli Contamination

    Marathon Ventures Inc is recalling Katy's Kitchen Roasted and Salted Sunflower Kernels due to potential E. coli contamination. The product was distributed to one customer in Nebraska.

    Product
    Katy's Kitchen Roasted and Salted Sunflower Kernals, Net Wt. 25 lbs,
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·19V133000·2019-02-27

    Triumph Recalls Motorcycles Due to Clutch Cable Wiring Damage Risk

    Triumph is recalling specific 2016-2019 motorcycles because the clutch cable may damage wiring, potentially causing electrical failures or engine stalling.

    Product
    TRIUMPH — TRIUMPH SCRAMBLER, STREET TWIN, BONNEVILLE T120 BLACK, STREET CUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0864-2019·2019-02-27

    Shimadzu TRINIAS Imaging Systems Recalled for Software and Display Errors

    Shimadzu is recalling 13 TRINIAS imaging systems due to software crashes and rare display corruption that may hinder medical examinations.

    Product
    TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0847-2019·2019-02-27

    bioMerieux Recalls VITEK 2 AST-N351 Test Kits Due to False Positives

    bioMerieux, Inc. is recalling VITEK 2 AST-N351 Test Kits distributed in the UK and Ireland because they may produce false positive results for ESBL phenotypes.

    Product
    VITEK 2 AST-N351 Test Kit
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0938-2019·2019-02-27

    Century Snacks Recalls Praline Pecans Due to Mispackaging

    Century Snacks LLC is recalling 25 packages of Praline Pecans because they were mispackaged with Praline Almonds. The error creates an undeclared allergen risk for consumers with nut allergies.

    Product
    Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040 centurysnacks.com
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·19V134000·2019-02-27

    Lexus Recalls 2018 LS Models for Run-Flat Tire Defect

    Toyota is recalling 2018 Lexus LS vehicles because run-flat tires may have cracked reinforcement layers, potentially causing tread separation and affecting vehicle stability.

    Product
    LEXUS — LEXUS LS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0845-2019·2019-02-27

    Medtronic Power Supply and Programmer Recall for Electrical Short Risk

    Medtronic is recalling 731 Power Supply 26907 and CareLink Encore 29901 Programmer units due to a potential electrical short circuit that can cause heating and smoke.

    Product
    Medtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 Programmer
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·19V140000·2019-02-27

    Midway Recalls One 2016 Freightliner Sprinter 3500 Wheelchair Lift Vehicle

    Midway Specialty Vehicles is recalling one 2016 Freightliner Sprinter 3500 because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2019·2019-02-27

    Ortho-Clinical Diagnostics Recalls VITROS VALP Reagent Packs Due to Negative Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products VALP Reagent Packs because they may produce negative bias results when measuring valproic acid.

    Product
    VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 6801710 INTENDED USE: For in vitro diagnostic use only. VITROS Chemistry Products VALP Reagent is used on the VITROS 5,1 FS Chemistry System, the VITROS 4600 Chemistry System and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2019·2019-02-27

    Boston Scientific Recalls Mislabelled Stingray Guidewires for Coronary Procedures

    Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.

    Product
    Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
    Category
    Medical Device
    Distribution
    Distributed nationwide