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.

30601–30625 of 50499

  • HighFDA (Food)·F-0052-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Tilapia Fillets for Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Tilapia Fillets in Texas, Louisiana, and Arkansas because they were produced with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Tilapia Fillet; UPC 234779 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each…
    Category
    Food
    Distribution
    3 states
  • HighCPSC·18025·2017-11-07

    Norco Recalls Children's Bicycles Due to Crank Failure Hazard

    Norco Bicycles is recalling specific children's models because the cranksets can bend or break during use, posing a fall hazard.

    Product
    Children's bicycles with Samox cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V699000·2017-11-06

    Forest River Recalls 2018 Puma Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Puma recreational trailers because the federal placards list incorrect tire size and pressure information, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V700000·2017-11-06

    Triumph Recalls 2016-2017 Speed Triple Motorcycles for Electrical Wiring Defect

    Triumph is recalling 2016-2017 Speed Triple S and R motorcycles because a charging system wire may rub against a bracket, potentially causing an electrical short and engine stall.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE S, SPEED TRIPLE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V695000·2017-11-03

    Entegra Motorhomes Recalled for Missing Exterior Reflectors

    Entegra is recalling 2016-2018 Aspire, Anthem, Cornerstone, and Insignia motorhomes because they lack required reflectors, reducing visibility to other drivers.

    Product
    ENTEGRA — ENTEGRA ANTHEM, ASPIRE, INSIGNIA, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V692000·2017-11-02

    Thor Motor Coach Recalls 2018 Motorhomes Due to Trailer Light Wiring Defect

    Thor Motor Coach is recalling 2018 Ace, Axis, Hurricane, Windsport, and Vegas motorhomes because trailer light wiring may be inserted incorrectly, causing lights to fail and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VEGAS, ACE, AXIS, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0032-2018·2017-11-01

    Kenny's Buckeye Pie Recalled for Undeclared Wheat

    Kenny's Great Pies, Inc. is recalling Buckeye Pies in Ohio due to undeclared wheat, a common allergen.

    Product
    Kenny's Buckeye Pie, Net Wt.22 oz. (624g).
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0046-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 1,152 bags of compounded Oxytocin 40 units in Lactated Ringer's USP because the drug was subpotent.

    Product
    Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only , Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-245-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V691000·2017-11-01

    Nissan Recalls 2017-2018 Infiniti QX30 for Air Bag Deployment Risk

    Nissan is recalling 2017-2018 Infiniti QX30 vehicles because the driver's air bag may deploy unexpectedly due to steering component grounding issues.

    Product
    INFINITI — INFINITI QX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0049-2018·2017-11-01

    FDA Requests Removal of Ablatherm Ultrasound System Software Settings

    FDA requested the removal of specific energy treatment settings from 12 Ablatherm ultrasound systems in the U.S. pending clinical data evaluation.

    Product
    Ablatherm(R) Integrated Imaging, High Intensity Ultrasound System For Prostate Tissue Ablation Transrectal high intensity focused ultrasound (HIFU) ablation of prostate tissue
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Drugs)·D-0039-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 390 bags of compounded Oxytocin 20 units in Lactated Ringer's Injection due to subpotent drug levels.

    Product
    Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0044-2018·2017-11-01

    Bard Max-Core Biopsy Instruments Recalled for Malfunction

    Bard Peripheral Vascular Inc is recalling 110,550 Max-Core Disposable Core Biopsy Instruments due to increased complaints of failure to prime, fire, or obtain samples.

    Product
    BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·17V690000·2017-11-01

    Heartland Recalls 2018 Pioneer Trailers Due to Propane Leak Risk

    Heartland is recalling 2018 Pioneer recreational trailers because the propane manifold block may be mounted too close to the shackle, creating a leak risk.

    Product
    HEARTLAND — HEARTLAND PIONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2018·2017-11-01

    Nucletron Oncentra Brachy 4.5 Software Recalled for Incorrect Source Step Size

    Nucletron BV is recalling Oncentra Brachy 4.5 radiation therapy software because incorrect source step sizes may occur in treatment plans.

    Product
    Oncentra Brachy 4.5 radiation therapy software The firm name on the label is Nucletron B.V. Oncentra is a radiation therapy planning software designed to analyze and plan radiation treatments in three dimensions for the purpose of treating patients with cancer. The treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0033-2018·2017-11-01

    Enlightened Pina Colada Ice Cream Recalled for Undeclared Coconut

    Beyond Better Foods is recalling Enlightened Pina Colada Ice Cream because it contains undeclared coconut, a major food allergen.

    Product
    ENLIGHTENED THE GOOD-FOR-YOU ICE CREAM 60 CALORIES PER SERVING PINA COLADA MORE PROTEIN. LESS SUGAR 1 PINT LOW FAT ICE CREAM, UPC 8 52109 33108 6. KEEP FROZEN.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0048-2018·2017-11-01

    GORE TAG Thoracic Endoprosthesis Recalled for Incomplete Deployment Risk

    W.L. Gore & Associates is recalling 12,197 GORE TAG Thoracic Endoprosthesis units worldwide due to a risk of incomplete or partial deployment during endovascular procedures.

    Product
    GORE TAG, THORACIC ENDOPROSTHESIS, CONFORMABLE. The GORE TAG Thoracic Endoprosthesis is intended for endovascular repair of all lesions of the descending thoracic aorta.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0040-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Lactated Ringer's Injection Bags

    Pharmedium Services, LLC is voluntarily recalling 978 bags of compounded Oxytocin in Lactated Ringer's Injection because the drug was subpotent.

    Product
    Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-103117·2017-10-31

    Trader Joe's Chicken Salads Subject to Listeria Public Health Alert

    USDA issued a public health alert for Trader Joe's broccoli slaw and kale salads with chicken due to possible Listeria contamination.

    Product
    Ghiringhelli Brothers — FSIS Issues Public Health Alert for Poultry Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·17V687000·2017-10-30

    MCI Recalls 2018 J4500 Buses Due to Incorrect Air Line Connections

    Motor Coach Industries is recalling 2018 MCI J4500 buses because air lines were incorrectly hooked to pressure gauges, potentially delaying driver response to low air conditions.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide