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.

3726–3750 of 52939

  • HighFDA (Devices)·Z-2424-2025·2025-09-03

    Canal filling stems recalled after unidentified substance found during retrospective evaluation

    ELEOS Segmental Stem Canal Filling straight slotted splined 2/3 plasma implants are recalled because an unidentified substance of unknown impact was found on devices. 15 units are affected.

    Product
    ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2471-2025·2025-09-03

    Hysterectomy procedure packs recalled over unconfirmed sterilization assurance requirements

    American Contract Systems robotic and vaginal hysterectomy packs are recalled because the firm cannot confirm that product sterilization assurance requirements were met. 50 units are affected.

    Product
    AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL/ITEM NUMBER GRRB10E; 2) VAG HYST PACK, MODEL/ITEM NUMBER SPVH62P.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·H-0534-2025·2025-09-03

    Everything bagel mix recalled because label omits sesame and other ingredients

    Baker's Authority Everything Bagel Mix in 1 lb and 5 lb bags is recalled because the label does not list its ingredients, including the major food allergen sesame. 197 units are affected.

    Product
    Baker's Authority Everything Bagel Mix; 5lb bag and 1lb bag; stored dry at room temperature; packaged in silver bag
    Category
    Food
    Distribution
    17 states
  • HighFDA (Food)·H-0537-2025·2025-09-03

    Friendly's ice cream recalled over undeclared wheat and soy from mismatched cartons

    Friendly's 48 fl oz cartons labeled Vanilla Bean carry a Cookies and Cream lid and contain Cookies and Cream, leaving wheat and soy undeclared. 54 cases are affected.

    Product
    Carton Label: "Friendly's Vanilla Bean"; 48 fl. oz. Lid Label: "Friendly's Cookies and Cream" Product in carton is Cookies and Cream.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0531-2025·2025-09-03

    Multigrain bread recalled because label omits sesame seed as allergen

    Breadman Bakery Multigrain bread, 24 oz, sold at seven Los Angeles retail locations, is recalled because the finished product label does not declare sesame seed. 52 loaves are affected.

    Product
    Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0548-2025·2025-09-03

    Bulk frozen shrimp recalled over insanitary conditions and possible cesium-137 contamination

    Frozen shrimp in bulk packaging is recalled because it was manufactured under insanitary conditions and may have been contaminated with Cesium-137. 17,214 cases across all brands are affected.

    Product
    Frozen shrimp in bulk packaging. 20 lbs (10 x 2 lbs blocks); 20 lbs (20 x 1 lbs blocks); 9 lbs case UPC# SH0176; SH0430; SH0320; SH0369; SH0370
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0603-2025·2025-09-03

    H-E-B alcohol pads recalled for isopropyl alcohol below labeled concentration

    H-E-B inControl Sterile Alcohol Pads, 100 per container, are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 300,000 pads.

    Product
    INCONTROL ALCOHOL — INCONTROL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·25V569000·2025-09-02

    Kenworth trucks display system may fail to show critical warnings

    PACCAR is recalling Kenworth T680, T880, and W990 trucks from 2024–2026 because the 15-inch digital display may fail to show warning lights or vehicle speed, increasing crash risk.

    Product
    KENWORTH — KENWORTH T680, T880, W990
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V568000·2025-09-02

    2025 Mazda CX-90: Inaccurate Fuel Gauge May Cause Unexpected Stalling

    Mazda is recalling certain 2025 Mazda CX-90 vehicles (also 2024 CX-90 and 2025 CX-70 mild hybrid models) because the fuel gauge may display an inaccurate reading, which could cause unexpected stalling and increase crash risk.

    Product
    MAZDA — MAZDA CX-70, CX-90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V564000·2025-08-29

    Tuff Trailer USA Recalls 2024 TTA17200T and TTA18200T Trailers

    Tuff Trailer USA is recalling 2024 TTA17200T and TTA18200T trailers because incorrect GVWR labels may lead to overloading and coupler failure.

    Product
    TUFF TRAILER USA — TUFF TRAILER USA TTA17200T, TTA18200T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E053000·2025-08-29

    Hiab Recalls Specific Reverse Hoists Due to Mounting Pin Failure Risk

    Hiab USA Inc. is recalling specific Galfab reverse hoists because a mounting pin may fail, allowing the hoist to fall and increasing the risk of injury.

    Product
    EQUIPMENT:MECHANICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V565000·2025-08-29

    Motorhome waste tank macerator fuse can overheat and melt housing

    REV Recreation Group is recalling certain American Coach, American Eagle, American Dream and Fleetwood Palisade RVs because the waste tank macerator fuse may overheat and melt the fuse housing.

    Product
    AMERICAN COACH — AMERICAN COACH, FLEETWOOD AMERICAN EAGLE, AMERICAN TRADITION, AMERICAN DREAM, PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25445·2025-08-28

    Carbon fiber road bicycle wheels recalled over structural integrity and crash hazard

    About 6,000 DT Swiss carbon fiber road wheels are recalled because a defect can compromise the wheel's structural integrity, posing a crash hazard. Six reports of carbon layer separation; no injuries reported.

    Product
    DT Swiss Carbon Fiber Road Wheels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25450·2025-08-28

    Lite-up torches and laser pointers recalled over accessible button cell batteries

    About 10,100 Party Favors lite-up torches and mini laser pointers are recalled because their button cell batteries can be accessed easily by children, in violation of mandatory standards. No incidents reported.

    Product
    Party Favors Lite-Up Torches and Mini Laser Pointers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25449·2025-08-28

    Coin battery chargers recalled because children can access the lithium batteries

    About 1,100 CT-ENERGY lithium coin battery chargers, model nc-02, are recalled because the coin batteries can be accessed easily by children and the packaging lacks child-resistance and the warnings required by Reese's Law.

    Product
    CT-ENERGY Lithium Coin Battery Chargers with Rechargeable 2032 Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25444·2025-08-28

    Locking carabiners recalled because the automatic closing mechanism can break

    About 12,600 Nimbus Lock Carabiners are recalled because the automatic closing mechanism can break and prevent the gate from closing, posing a fall risk. There are 21 reports of breakage; no injuries reported.

    Product
    Nimbus Lock Carabiners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2331-2025·2025-08-27

    Bayonet injection needles recalled after showing elevated cytotoxicity in testing

    Bayonet Luer-Lock injection needles, models 50-353-23 and 50-345-23, are recalled because affected product showed elevated cytotoxicity values, which may present a risk of intolerance or allergic reaction.

    Product
    Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile; 2. Model no. 50-345-23, working length 24 cm, total length 31 cm, non-sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0505-2025·2025-08-27

    Ojasvita Chocomalt 200 g pouches recalled for undeclared soy lecithin

    Sri Sri Tattva Ojasvita Chocomalt, 7 oz / 200 g paper pouches, is recalled because it contains undeclared soy lecithin. 1,100 units are affected.

    Product
    Sri Sri Tattva, Ojasvita Chocomalt,7oz / 200g, Paper Pouch, 25 packages per case
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·H-0504-2025·2025-08-27

    Zero sugar soda cans recalled because they contain full sugar product

    7up Zero Sugar Tropical Soda in 12 fl oz cans is recalled because the cans are labeled Zero Sugar but contain full sugar product. 1,954 cases are affected.

    Product
    7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0591-2025·2025-08-27

    Sodium bicarbonate injection vials recalled for lack of assurance of sterility

    Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide