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.

15201–15225 of 53092

  • HighFDA (Devices)·Z-0358-2023·2022-12-14

    Dover Urinary Catheter Drainage Tray Recall Due to Blockage Risk

    Cardinal Health is recalling Dover Closed Urethral Tray urinary drainage systems due to potential blockage of the drainage bag inlet port, which may prevent proper bladder emptying and increase the risk of urinary retention.

    Product
    Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 14 Fr/Ch (4.7 mm) Product Code: 3410 Intended for urinary drainage from the bladder of a patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0187-2023·2022-12-14

    Taylor Farms Jicama Sticks recalled due to metal fragment contamination

    Taylor Farms Northwest is recalling 539 units of Taylor Farms Jicama Sticks because a metal fragment was found in a package. The product was distributed in Washington with sell-by dates of 11/13/2022 through 11/17/2022.

    Product
    Taylor Farms Jicama Sticks, Refrigerated & Ready To Eat product, packaged in a clear plastic clamshell container, net wt. 14 oz. Distributed by Taylor Farms NW Kent, WA 98032. UPC 30223 11248.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0190-2023·2022-12-14

    Weis Quality Premium Ice Cream Recalled for Undeclared Soy and Coconut

    Weis Quality ice cream contains undeclared soy and coconut allergens. Consumers with allergies should discard or return the product.

    Product
    Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0418-2023·2022-12-14

    Spinal Implant Screws Recalled Due to Potential Weld Failure

    LineSider Spinal System screws are recalled due to potential weld separation between components that could cause the Tulip Head to detach from the Screw Shank. The recall affects 1,227 screws distributed nationwide.

    Product
    LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0188-2023·2022-12-14

    Taylor Farms Guacamole Tray Recalled for Metal Fragment

    Taylor Farms is recalling its 61 oz Guacamole Tray because a metal fragment approximately 3/4 inch was found in a retail package. The recall affects 161 units distributed in Washington.

    Product
    Taylor Farms Guacamole Tray - Large, Refrigerated & Ready To Eat product, packaged in a plastic round container, net wt. 61 oz. The tray contains Cucumber, Baby Carrots, Jicama, Red Bell Pepper, Yellow Bell Pepper, and Blended Guacamole (Hass Avocados). Distributed by Taylor…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0413-2023·2022-12-14

    Bipolar Forceps Recall: Incomplete Instructions for Surgical Device

    BD recalls CareFusion bipolar forceps (Ref F-5301) due to incomplete Instructions For Use. The IFU is missing information about power supply interface and cleaning and maintenance.

    Product
    CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.5MM TIP, STRAIGHT, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5301
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0359-2023·2022-12-14

    Dover Closed Urethral Tray Recalled Due to Drainage Port Blockage Risk

    Cardinal Health recalls Dover Closed Urethral Tray due to potential blockage of the urinary drainage bag inlet port that could prevent urine drainage and increase risk of urinary retention if bladders are not emptied timely.

    Product
    Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Intended for urinary drainage from the bladder of a patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0193-2023·2022-12-14

    Big Sky Chocolate Chunk Granola Recalled for Undeclared Milk Allergen

    SUBURBAN BREAD CO. is recalling Big Sky Chocolate Chunk Granola (14oz pouches) because product labeling fails to declare milk, a sub-ingredient present in the granola. This poses a risk to consumers with milk allergies.

    Product
    Big Sky Chocolate Chunk Granola, Net Wt 14oz; UPC 02503 00475
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V922000·2022-12-13

    2023 Jayco Solstice defrost controls may fail, increasing crash risk

    Jayco is recalling 2023 Solstice and Entegra Expanse recreational vehicles because the HVAC system's defrost and defog controls may stop working. This loss of visibility control increases the risk of crashes under certain driving conditions.

    Product
    ENTEGRA — ENTEGRA, JAYCO EXPANSE, SOLSTICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V920000·2022-12-13

    2023 Forest River Travel Trailers Recalled for Refrigerator Wiring Fire Risk

    Forest River is recalling certain 2023 Wildwood, Salem, and Stealth EVO travel trailers. The 8-gauge refrigerator wire lacks over-current protection, creating a fire risk from melted wiring.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, STEALTH EVO, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23066·2022-12-12

    Art of Green Laundry Detergent Recalled for Bacterial Contamination

    AlEn USA is recalling Art of Green laundry detergent products because they may contain Pseudomonas aeruginosa bacteria, which can cause serious infection in people with weakened immune systems or external medical devices.

    Product
    Art of Green laundry detergent products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V919000·2022-12-12

    Freightliner and Western Star trucks recalled for tire incompatibility

    Daimler Trucks is recalling certain Freightliner and Western Star commercial trucks with tires incompatible with their 8.25-inch rims. Incompatible tires can reduce performance and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 122SD, 114SD, BUSINESS CLASS M2, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V912000·2022-12-09

    Kawasaki Recalls Motorcycles Due to Camshaft Chain Tensioner Defect

    Kawasaki is recalling specific 2015-2023 motorcycles because a defective camshaft chain tensioner may lock, causing the engine to stall while riding.

    Product
    KAWASAKI — KAWASAKI Z H2, NINJA H2 SX, NINJA H2, NINJA 1000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V911000·2022-12-09

    Braun Ambulances Recall 2014-2022 Models Due to HVAC Fire Risk

    Braun Ambulances is recalling 1,321 vehicles from 2014-2022 because a faulty relay may cause the HVAC system to overheat, increasing the risk of a fire.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES PATRIOT, EXPRESS, CHIEF XL, SIGNATURE SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V907000·2022-12-08

    Subaru Ascent 2019–2022 Recall for Electrical Fire Risk

    Subaru is recalling 2019–2022 Ascent vehicles due to an improperly fastened ground bolt on the PTC heater that could melt and cause an electrical fire.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V904000·2022-12-08

    2019-2022 RAM Pickup Trucks Recalled for Defective Tailgate Latch

    Chrysler is recalling 2019-2022 RAM 1500, 2500, and 3500 pickup trucks because the tailgate may not latch properly due to misaligned strikers. An unintended tailgate opening while driving could result in cargo loss and increased crash risk.

    Product
    RAM — RAM 3500, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23057·2022-12-08

    Cordless Window Shades Battery Packs Recalled for Fire Hazard

    About 56,000 lithium-ion battery packs used in cordless window blinds are being recalled because they can overheat and pose a fire hazard. The firm has received reports of overheating and one fire in a commercial warehouse, though no consumer injuries have been reported.

    Product
    Cordless Window Shades Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V909000·2022-12-08

    School buses recalled for incorrectly tightened rear axle fasteners

    Navistar is recalling certain 2023-2024 IC BUS school buses due to fasteners on the rear axle that may have been tightened incorrectly. This can allow the rear axle to shift, reducing vehicle control and increasing crash risk.

    Product
    IC BUS — IC BUS CESB, RESB, EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V903000·2022-12-08

    GM recalls multiple 2020-2023 vehicles for daytime running light control defect

    General Motors is recalling multiple 2020-2023 models because daytime running lights may fail to turn off when headlights are on, creating glare and visibility hazards.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SILVERADO 1500, SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0354-2023·2022-12-07

    Alcon Surgical Procedure Packs Recalled for Adhesive Defect and Skin Injuries

    Alcon is recalling Custom Pak Surgical Procedure Packs because the adhesive liner is difficult to remove and the manufacturer has observed an increase in skin injuries related to the adhesive.

    Product
    Alcon Custom Pak Surgical Procedure Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0324-2023·2022-12-07

    CoViPoint COVID Test Kits Distributed Without FDA Approval or Clearance

    GS Biomark LLC distributed approximately 639,200 CoViPoint COVID test kits without FDA approval, clearance, or authorization across multiple US states.

    Product
    CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200 BM-D4K0200 BM-DK0200 BM-DK0600 BM-DK0800 BM-DK1200 BM-DK1400 BM-DK1800
    Category
    Medical Device
    Distribution
    11 states