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.

29751–29775 of 50499

  • HighFDA (Devices)·Z-0776-2018·2018-03-07

    Philips Intellivue iX Software Recall for Patient Discharge Failure

    Philips is recalling Intellivue iX Information Center Software because restarting stations in 2018 prevents patient discharge and transfer operations, causing monitoring loss.

    Product
    Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 IntelliVue Info Center iX A.0 866117 PIIC Classic Upgrade 866389 IntelliVue Info Center iX B.0, C.0 867141 IntelliVue Info Center iX B.0 866025 IntelliVue Server IX A.0 866118…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0783-2018·2018-03-07

    Avid Medical Recalls Pacemaker Tray Kits with Foreign Material

    Avid Medical is recalling 70 TruCustom Pacemaker Tray kits because they may contain needles with loose polypropylene foreign material.

    Product
    AVID TruCustom PACEMAKER TRAY convenience kits, Item Code: LAKC020-08 and LAKC020-09
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-0832-2018·2018-03-07

    Sumano's Bakery Recalls Sourdough French Bread Due to Metal Contamination

    Sumano's Bakery is recalling Sourdough French bread after a customer found a small metal piece on the outside of the loaf before baking.

    Product
    Sourdough French: Product number 2044; SKU 61659799; GTIN [00046567600932] ; UPC 831 49000044 20 pieces; Ingredients: Unbleached Wheat Flour, Water, Sea Salt, Starter (Fermented dough). Best Practices: 1. Keep Bread frozen at all times 2. Pull bread out of freezer…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0699-2018·2018-03-07

    Moog Curlin Infusion Administration Set Recalled Due to Particulate Matter

    Zevex Incorporated is recalling specific lots of Moog Curlin Infusion Administration Sets because particulate matter was found on the spike.

    Product
    MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site with Check Valve, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0809-2018·2018-03-07

    Aesculap proSA Tool Set Recalled for Incorrect Valve Pressure Adjustment

    Aesculap Implant Systems LLC is recalling proSA Tool Sets because the adjusting pin does not set the correct valve opening pressure for the shunt system.

    Product
    proSA Tool Set used to adjust and verify the proSA Adjustable Shunt System Shunt, central nervous system and components
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0792-2018·2018-03-07

    Avid Medical Recalls TruCustom Laminectomy Kits Due to Foreign Material

    Avid Medical is recalling 12 TruCustom Laminectomy Kits because they may contain needles with loose polypropylene foreign material.

    Product
    AVID TruCustom LAMINECTOMY PACK convenience kits, Item Code: MADN013-02
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-0839-2018·2018-03-07

    M&P Food Productions Recalls Blintzes for Undeclared Wheat and Red Dye

    M&P Food Productions is recalling Hand Made Russian Style Blintzes because they contain undeclared wheat and FD&C Red #40.

    Product
    M&P Food Productions brand Hand Made Russian Style Blintzes, (6 pieces): Cheese and Cherry, Net Wt. 14 oz. (396g), UPC Codes: 7 07163 30327 5, Keep Frozen
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0722-2018·2018-03-07

    Zimmer Biomet Recalls Versys Hip Prostheses Due to Sterile Barrier Risk

    Zimmer Biomet is recalling 38,069 units of Versys 6 inch Beaded Full Coat Plus Hip Prostheses because weight issues may have compromised the sterile barrier.

    Product
    Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled as follows: a. VERSYS 6 INCH BEADED FC 19X160MM STD BODY STD NECK (Item No. 00894301906); b. VERSYS 6 INCH BEADED FC 21X160MM STD BODY STD NECK (Item No. 00784302106); c. VERSYS 6 INCH BEADED FC 22X160MM STD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0867-2018·2018-03-07

    Kanan Enterprises Recalls Unsalted Almonds Due to Undeclared Allergens

    Kanan Enterprises is recalling Southern Grove Unsalted Almonds because some bags contained Wasabi Soy Almonds, which include undeclared wheat, soy, and peanut oil.

    Product
    SOUTHERN GROVE ALMONDS Unsalted 14 oz (397g) pouch bag INGREDIENTS: ALMONDS. Distributed by ALDI Inc. Batavia, IL 60510 UPC 0 41498 24647 1
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0717-2018·2018-03-07

    Philips Allura Xper FD X-ray Systems Recalled for Monitor Fall Hazard

    Philips is recalling 1,486 Allura Xper FD and ORT X-ray systems because extra monitors mounted on the ceiling suspension may disengage and fall.

    Product
    Allura Xper FD and and Xper FD ORT - Philips X-ray Systems Product Usage: The Allura Xper FD10 and Alllura Xper FD10/10 is intendd for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18114·2018-03-06

    Woodstream Recalls Mosquito Magnet Traps Due to Injury Hazard

    Woodstream is recalling Mosquito Magnet traps because cleaning them with Quick Clear Cartridge kits can cause the regulator to break and propel pieces, posing an injury risk.

    Product
    Mosquito Magnet traps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18116·2018-03-06

    InSinkErator Recalls SinkTop Switches for Garbage Disposals Due to Fire Hazard

    InSinkErator is recalling about 1.4 million SinkTop switches for garbage disposals because water can enter the power module, posing a fire hazard. No injuries have been reported.

    Product
    InSinkErator Single Outlet SinkTop Switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V147000·2018-03-06

    Alfa Romeo Stelvio Recalled for Wiper Motor Software Defect

    Chrysler is recalling 2018 Alfa Romeo Stelvio vehicles because wiper motor software may limit wipers to low speed, reducing visibility and increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V153000·2018-03-06

    Nissan Recalls 2018 370Z Vehicles Due to Driver's Side Air Bag Defect

    Nissan is recalling 2018 370Z vehicles because the driver's side curtain air bag may be installed incorrectly, potentially preventing proper deployment in a crash.

    Product
    NISSAN — NISSAN 370Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V145000·2018-03-05

    Morgan Truck Bodies Recalled for Turn Signal Wiring Defect

    Morgan Truck Bodies LLC is recalling 2013-2018 models because water may enter the wiring harness, affecting turn signal operation and increasing crash risk.

    Product
    MORGAN — MORGAN TRUCK BODIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V146000·2018-03-05

    Triple E Recalls 2017-2018 Motorhomes Due to Incorrect Cargo Capacity Labels

    Triple E is recalling 2017-2018 Unity, Wonder, and Serenity motorhomes because incorrect labels may indicate higher cargo capacity than actual, increasing crash risk.

    Product
    TRIPLE E — TRIPLE E, TRIPLE E RV UNITY, SERENITY, WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V144000·2018-03-02

    Newmar Recalls 2018 Essex Motorhomes Due to Taillight Detachment Risk

    Newmar is recalling 2018 Essex motorhomes because taillights may loosen and detach while driving, increasing crash risk. Dealers will secure the lights with new hardware.

    Product
    NEWMAR — NEWMAR ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18112·2018-03-01

    Graco Recalls Table2Table Highchairs Due to Rear Leg Fall Hazard

    Graco is recalling about 36,000 Table2Table 6-in-1 highchairs sold at Walmart because the rear legs can pivot out of position, creating a fall hazard.

    Product
    Graco Table2Table 6-in-1 Highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V142000·2018-03-01

    Coach House Recalls RVs with Defective Kidde Fire Extinguishers

    Coach House is recalling 2003-2018 recreational vehicles equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.

    Product
    COACH HOUSE — COACH HOUSE ARRIVA, PLATINUM II, PLATINUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V141000·2018-03-01

    Ford Recalls 2017-2018 Taurus Vehicles for Ignition Key Removal Defect

    Ford is recalling 2017-2018 Taurus vehicles because the ignition key may be removed when the transmission is not in Park, increasing the risk of the vehicle rolling away.

    Product
    FORD — FORD TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V139000·2018-03-01

    Land Rover Recalls 2018 Range Rover Velar for Visibility Defect

    Jaguar Land Rover is recalling 2018 Range Rover Velar vehicles because ventilation system parts may detach, preventing fog removal from windows and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E011000·2018-03-01

    RockyMounts Recalls Four Bicycle Rack Models Due to Weld Failure Risk

    RockyMounts is recalling four bicycle rack models because a weld may crack, causing the rack and bicycles to separate from the vehicle and create a road hazard.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide