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.

10201–10225 of 22145

  • HighFDA (Food)·F-1787-2024·2024-09-11

    Apple Danish Recalled for Incorrect Almond Croissant Ingredient Labeling

    SSP America PHX is recalling Apple Danish products due to incorrect ingredient labeling. The label lists Almond Croissant ingredients instead of Apple Danish, creating a risk for consumers with tree nut allergies.

    Product
    Apple Danish in a clear plastic bag with a white paper label attached to the top of the plastic bag.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0650-2024·2024-09-11

    Compounded semaglutide injection recalled due to sterility concerns

    ProRx LLC is recalling compounded semaglutide injections due to lack of assurance of sterility. The recall affects 2,490 vials distributed nationwide.

    Product
    Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V594000·2024-09-08

    Ford windshield wiper motor failure recall affects Mach-E and other models

    Ford is recalling certain 2023–2024 Mustang Mach-E, Maverick, and Bronco Sport vehicles because the windshield wiper motor may become inoperative, reducing visibility and increasing crash risk. Dealers will replace the motor free of charge.

    Product
    FORD — 2023 FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V590000·2024-09-08

    2022 Ford Maverick Electrical System Defect Increases Crash Risk

    Ford is recalling certain 2022 Mavericks due to a defect in body and power train control modules that may fail to detect changes in 12-volt battery charge, potentially resulting in loss of hazard lights or drive power and increasing the risk of crashes.

    Product
    FORD — 2022 FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V597000·2024-09-08

    2024 Ford Ranger Power Windows May Not Reverse When Detecting Objects

    Ford is recalling 2024 Ranger vehicles because power windows may fail to automatically reverse when detecting an object, risking pinching injuries to occupants.

    Product
    FORD — 2024 FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V523000·2024-09-07

    Prevost buses recalled for defective wheelchair lift bridging device

    Prevost recalls certain 2005-2024 buses with wheelchair lifts due to a potentially steep bridging device that can cause wheelchair instability. Affected owners should contact Prevost for a free replacement.

    Product
    PREVOST — 2014 PREVOST H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V506000·2024-09-07

    2023 Ford Super Duty Trucks and Escape Instrument Panel Illumination Defect

    Ford is recalling certain 2023 Super Duty F-250, F-350, F-450, F-550 and Escape models. The instrument panel module may fail to illuminate due to improper soldering, preventing drivers from seeing critical safety information like the speedometer and warning lights.

    Product
    FORD — 2023 FORD F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V507000·2024-09-07

    2023 Ford Super Duty Trucks Door Window Auto-Reverse May Fail

    Ford is recalling 2023 Super Duty F-250, F-350, F-450, and F-550 trucks due to a door module power issue that may prevent the power window anti-pinch function from detecting obstructions and automatically reversing.

    Product
    FORD — 2023 FORD F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V510000·2024-09-07

    2023 Ford F-53 and F-59 Recalled for Inoperative Instrument Panel

    Corrosion in the Smart Data Link Connector may prevent the instrument panel from displaying critical safety information like the speedometer and warning lights in certain 2023 Ford F-53 and F-59 vehicles, increasing crash risk.

    Product
    FORD — 2023 FORD F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V504000·2024-09-07

    Peterbilt and Kenworth trucks recalled for loose driveline fasteners

    PACCAR is recalling certain 2023-2024 Peterbilt and Kenworth trucks due to improperly applied thread-lock on driveline fasteners. Loose fasteners could allow the driveline to separate, increasing crash risk.

    Product
    PETERBILT — 2023 PETERBILT 537
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V437000·2024-09-06

    2023 Volkswagen GTI and Golf R suspension strut mount defect

    Volkswagen is recalling certain 2023 GTI and Golf R vehicles due to deformed suspension strut mounts that may loosen and cause steering instability. Dealers will replace affected components at no cost.

    Product
    VOLKSWAGEN — 2023 VOLKSWAGEN GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V436000·2024-09-06

    2022 Volkswagen ID.4 Recalled for Rearview Camera Software Defect

    Volkswagen is recalling 2022 ID.4 vehicles with defective rearview camera software. The defect can delay or deactivate the rearview camera image, reducing rear visibility and increasing crash risk.

    Product
    VOLKSWAGEN — 2022 VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V321000·2024-09-05

    Honda Ridgeline rearview camera wire harness subject to fatigue and failure

    Honda is recalling 2020–2024 Ridgeline vehicles because the rearview camera wire harness may fatigue and break, preventing the camera image from displaying and reducing rear visibility.

    Product
    HONDA — 2024 HONDA RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24354·2024-09-05

    Delta Cycle Ceiling Hoists with Straps Recalled for Buckle Breakage Injury Risk

    Delta Cycle Corp is recalling ceiling hoists with straps because plastic buckles can break when holding kayaks, canoes, or other large objects. The company has received four incident reports, including one minor injury.

    Product
    Ceiling Hoists with Straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V319000·2024-09-05

    2024 Rivian R1S and R1T recalled due to missing airbag warning label

    Rivian is recalling 2024 R1S and R1T vehicles with missing dashboard airbag warning labels. The missing label may prevent drivers from understanding airbag safety risks to children in the front seat.

    Product
    RIVIAN — 2024 RIVIAN R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2770-2024·2024-09-04

    Medical procedure kits recalled due to defective plastic syringes

    Medline's Centurion procedure kits are being recalled due to plastic syringes with leaks and breakage. The defective syringes may pose a risk to patient health during medical procedures.

    Product
    Centurion procedure kits labeled as: 1) BONE MARROW TRAY, Pack Number SPEC0255; 2) CT/ULTRASOUND BIOPSY, Pack Number SPEC0262; 3) FINE LACERATION KIT, Pack Number SUT17215; 4) INFECTION DRIVELINE MANAGEMENT KIT, Pack Number DM645; 5) LACERATION TRAY, Pack Number DYNDL1
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2730-2024·2024-09-04

    Stryker iBur surgical bur may overheat during bone-cutting procedures

    Stryker iBur 3.0mm Diamond Match Head surgical cutting tools may reach temperatures exceeding safe operating limits during bone surgery, potentially causing thermal tissue injury. About 2,507 units worldwide are affected.

    Product
    Stryker iBur 3.0mm Diamond Match Head, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2614-2024·2024-09-04

    Pediatric Tracheostomy Tubes Recalled Due to Defective Securement Flange

    Smiths Medical recalls pediatric tracheostomy tubes from specific lots due to a manufacturing defect that may cause the securement flange to tear. No injuries have been reported.

    Product
    a) PEDIATRIC TRACHEOSTOMY TUBE 2.5mm TTS FLEXTEND STRAIGHT NECK , Product Code/List Number/Item Code 67PFSS25; b) PEDIATRIC TRACHEOSTOMY TUBE 3.0mm TTS FLEXTEND STRAIGHT NECK , Product Code/List Number/Item Code 67PFSS30; c) PEDIATRIC TRACHEOSTOMY TUBE 3.5mm TTS FLEXTEND STRA
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2771-2024·2024-09-04

    Breast biopsy kits recalled due to defective syringes with leaks and breakage

    Medline Industries recalls Centurion breast biopsy procedure kits due to defective plastic syringes that may leak or break. The syringes are affected by an FDA safety alert and pose potential risks during medical procedures.

    Product
    Centurion procedure kits, labeled as: 1) BREAST BIOPSY KIT, Pack Number MNS6950A; 2) BREAST BIOPSY PACK, Pack number BT515A
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1751-2024·2024-09-04

    Infant Formula Recalled Due to Excess Vitamin D Levels

    CVS Health and HEB Baby Premium Infant Formula with Iron is recalled due to vitamin D levels exceeding permitted maximums. The recall affects 16,500 units.

    Product
    CVS Health brand and HEB Baby brand Premium Infant Formula with Iron Milk-Based Powder; packaged in 964g composite cans; 4 cans per case; UPC 50428318034 and 41220164578
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-2780-2024·2024-09-04

    Centurion Procedure Packs with Defective Syringes Recalled Worldwide

    MEDLINE INDUSTRIES is recalling Centurion procedure packs containing syringes with documented leaks, breakage, and other quality defects. The affected syringes may pose a risk to patient health during medical procedures.

    Product
    Centurion procedure packs, containing Caina syringes, labeled as: 1) BREAST BIOPSY KIT, Pack Number DYNDH1512A; 2) CIRCUMCISION KIT, Pack Number CIT6535; 3) CIRCUMCISION KIT, Pack Number CIT7095; 4) CIRCUMCISION TRAY, Pack Number CIT6860A; 5) CIRCUMCISION TRAY, Pack N
    Category
    Medical Device
    Distribution
    0 states