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.

17976–18000 of 50404

  • HighFDA (Devices)·Z-0653-2022·2022-02-23

    Smiths Medical Medfusion Syringe Infusion Pumps Recalled for Alarm System Failures

    Smiths Medical is recalling certain Medfusion syringe infusion pumps due to intermittent alarm system failures that may occur during power-on self-tests outside the warranty period.

    Product
    Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion Pumps serviced during the same time period in which a main board was replaced using replacement main board part numbers G6000361, G6000435, G6001260, G6001560, G6001562 and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0735-2022·2022-02-23

    Frozen Chopped Spinach Recalled for Possible Listeria Contamination

    Steamable by Lidl Chopped Spinach is recalled due to possible Listeria monocytogenes contamination. Affected products were distributed to Lidl stores across eight states.

    Product
    Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Frozen product.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0651-2022·2022-02-23

    Exeter V40 Cemented Hip Stem Recalled for Potential Label Mix-Up

    Howmedica Osteonics is recalling Exeter V40 Cemented Hip (125mm) Stem devices due to a potential label mix with 150mm stems. Incorrect labeling could result in wrong implant size being used during surgery.

    Product
    Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0642-2022·2022-02-23

    Dental Resin Product Recalled Due to Non-Registered Manufacturing and Mislabeling

    Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.

    Product
    FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0646-2022·2022-02-23

    Destino Twist and Guidestar Devices Recalled for Potential Threaded Component Separation

    Oscor Inc. is recalling 549 units of Destino Twist and Guidestar devices due to potential separation between the threaded hub and cap. Affected devices were distributed in Tennessee, Pennsylvania, and the Czech Republic.

    Product
    Destino Twist 14F (also branded as Guidestar 14F)
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0736-2022·2022-02-23

    Pretty Thai Sweet Chili Sauce Recalled for Undeclared Peanuts

    Pretty Thai Sweet Chili Stir Fry & Barbecue Sauce is being recalled due to potential undeclared peanuts. Consumers with peanut allergies should not consume the product.

    Product
    Pretty Thai Sweet Chili Stir Fry & Barbecue Sauce NET WT. 11.2 oz (317g) UPC 860043001224 packaged in a cylindrical clear PET plastic bottle
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0638-2022·2022-02-23

    Endoscope Reprocessor Tubing Assembly Error May Reduce Disinfection Effectiveness

    Olympus OER-Elite Endoscope Reprocessors may have incorrectly assembled detergent and alcohol tank tubing, causing solutions to be dispensed in reversed cycles. This results in ineffective endoscope disinfection and potential patient exposure to residual detergent.

    Product
    OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes, their accessories, and endoscope reprocessor accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0640-2022·2022-02-23

    Liko Mobile Patient Lifts Recalled for Missing Bushings and Wear Risk

    Hill-Rom is recalling 1,215 Liko M220 and M230 mobile patient lifts with missing bushings that cause wear and risk of patient falls. Units were distributed worldwide.

    Product
    Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22087·2022-02-23

    Bebe au Lait Wooden Teethers Recalled for Choking Hazard

    Bebe au Lait is recalling approximately 8,600 wooden teethers because the string connecting beads can come untied, releasing beads that pose a choking hazard to young children. The company has received six reports of detached beads, including one case where a child placed a bead in their mouth.

    Product
    Wooden Teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V105000·2022-02-23

    2022 Keystone Cougar Tires: Load Range Defect Increases Crash Risk

    Keystone RV recalls 2022 Cougar trailers with incorrectly specified tires. Load Range D tires were installed instead of required Load Range E, creating overload and crash risk.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0639-2022·2022-02-23

    Liko M220 mobile lifts recalled for missing bushing, fall risk

    Hill-Rom is recalling 5,470 Liko M220 mobile lifts used in nursing homes due to a missing bushing that can cause wear and potentially lead to patient falls.

    Product
    Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0652-2022·2022-02-23

    Exeter V40 Cemented Hip Stem Labels May Mismatch Between Sizes

    The FDA has recalled Exeter V40 Cemented Hip (150mm) Stems due to a potential labeling mix-up with the 125mm version. Patients who received the device should verify with their surgeon that the correct size was implanted.

    Product
    Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0649-2022·2022-02-23

    Wireless Foot Switch Firmware Issue in Philips Veradius Unity Devices

    The wireless foot switch in Philips Veradius Unity medical systems can lose function due to a firmware issue. This could cause delays or interruption of medical procedures if alternative input methods are not used.

    Product
    Veradius Unity, Model #718132
    Category
    Medical Device
    Distribution
    26 states
  • HighNHTSA·22E013000·2022-02-23

    Comoto Recalls Bilt Motorcycle Helmets for Impact Protection Defect

    Comoto is recalling specific Bilt motorcycle helmets that may not adequately protect the wearer during a head impact, failing federal safety standards.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22086·2022-02-23

    Festive Lights Hanukkah Menorahs Recalled Due to Fire Hazard

    The TJX Companies is recalling about 7,900 Festive Lights Hanukkah Menorahs because the resin and MDF material can burn or catch fire when holding lit candles. Three incidents of burning or catching fire have been reported, with no injuries or property damage.

    Product
    Festive Lights Hanukkah Menorahs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V101000·2022-02-22

    2022 Freightliner Cascadia brake system failure and parking brake defect

    Daimler Trucks North America is recalling 2022 Freightliner Cascadia trucks for a software and brake hardware defect that may cause loss of braking and parking brake functionality, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·007-2022·2022-02-22

    Frickenschmidt Recalls Teriyaki Beef Sticks Due to Gluten Mislabeling

    Frickenschmidt Foods LLC is recalling ready-to-eat teriyaki beef sticks because they are labeled 'gluten free' but contain wheat. No adverse reactions have been reported.

    Product
    Lockwood Packing CO, LLC — Frickenschmidt Foods LLC Recalls Ready-to-Eat Beef Stick Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V099000·2022-02-22

    Mercedes-Benz Metris Recalled for Rearview Camera Display Freeze

    Daimler Vans USA is recalling 2015-2018 Mercedes-Benz Metris vehicles because a defective memory chip may cause the rearview camera image to freeze, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E011000·2022-02-21

    Joyson Recalls Curtain Air Bag Inflators Due to Component Errors

    Joyson is recalling specific curtain air bag inflators because production interruptions may have caused duplicate or missing components, potentially affecting crash performance.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN:INFLATOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V094000·2022-02-18

    Thor Motor Coach Omni and Magnitude motorhomes recalled for LP gas line fire hazard

    Thor Motor Coach is recalling certain 2020-2021 Omni and Magnitude motorhomes due to incorrectly routed LP gas lines that could damage and cause a gas leak, increasing fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OMNI, redundant MAGNITUDE, redundant OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V097000·2022-02-18

    Lance Recalls 2022 Travel Trailers Due to Propane Hose Fire Risk

    Lance Camper is recalling 2022 1685 and 1985 travel trailers because an improperly secured propane hose may contact leaf springs, causing a gas leak and increasing fire risk.

    Product
    LANCE — LANCE 1985, 1685
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22727·2022-02-17

    Husqvarna All-Wheel Drive Robotic Lawnmowers Recalled for Fire Hazard

    Husqvarna is recalling about 1,400 Automower 435X and 535 all-wheel drive robotic lawnmowers because the lithium-ion battery can overheat and catch fire. The company has received five reports of battery overheating, including two fires.

    Product
    Husqvarna Automower 435X and 535 All-Wheel Drive Robotic Lawnmowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22729·2022-02-17

    Polaris Model Year 2022 Snowmobiles Recalled for Crash Hazard

    Polaris Industries is recalling approximately 7,400 Model Year 2022 MATRYX snowmobiles because the throttle release switch can fail to disengage or the throttle cable can be kinked, posing a crash hazard.

    Product
    Model Year 2022 MATRYX RMK, INDY, SWITCHBACK, VOYAGEUR, and NORDIC PRO snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide