The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

Agency

Category

Minimum severity

Clear filters

6251–6275 of 90258

  • HighFDA (Devices)·Z-2440-2025·2025-09-03

    Custom loupes with Dragonfly frames recalled over nickel nose pad allergy risk

    Orascoptic custom loupes with Dragonfly frames are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 15,245 units are affected.

    Product
    Orascoptic Superior Visualization Custom loupes with Dragonfly frames
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0601-2025·2025-09-03

    CURAD alcohol prep pads recalled for isopropyl alcohol below labeled strength

    CURAD Sterile Alcohol Prep Pads, medium 2-ply, are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 1,639,996 pads.

    Product
    CURAD ALCOHOL PREP PADS — CURAD ALCOHOL PREP PADS (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2452-2025·2025-09-03

    Surgery trays recalled because they contain recalled tourniquet cuffs

    Medline General Surgery Trays are recalled because they contain recalled Stryker Color Cuff tourniquet cuffs whose flange may detach, compromising air pressure and risking tourniquet failure. 1,145 units are affected.

    Product
    The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and includes a range of components dependent upon the specific procedure. These kits will be assembled using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0546-2025·2025-09-03

    Ice cream cartons recalled over undeclared almond, walnut and pecan

    Chocolate Chip Cookie Dough ice cream in half gallon cartons carrying a Moo-llennium Crunch lid is recalled for undeclared almond, walnut and pecan. 16,532 half gallons are affected.

    Product
    Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. Packaging contains Moo-llennium crunch. Packaged in half gallon cartons (1.89 L)
    Category
    Food
    Distribution
    17 states
  • HighNHTSA·25E054000·2025-09-03

    Magna Recalls Rearview Cameras on Ford and Chrysler Vehicles

    Magna International is recalling rearview cameras installed on certain Ford and Chrysler vehicles because they may display a blank or inverted image, increasing crash risk.

    Product
    BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0549-2025·2025-09-03

    Raw frozen shrimp recalled over possible contamination with cesium-137

    Great Value and Sea Best branded raw frozen shrimp in bulk master cartons, product of Indonesia, is recalled because the product may be contaminated with Cesium-137. 33,164 pounds are affected.

    Product
    Great Value branded and Sea Best branded raw frozen shrimp in bulk packaging, master cartons. Master carton case is 20 lbs (10 x 2lbs retail bags), and 18 lbs (12 x 1.5lbs retail bags) and (10x1lb retail bags), Product of Indonesia, Keep Frozen, Distributed by Beaver Street…
    Category
    Food
    Distribution
    3 states
  • 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 (Drugs)·D-0598-2025·2025-09-03

    Sucralfate tablets recalled after bankruptcy left quality program unmonitored

    Sucralfate Tablets USP 1 gram from American Health Packaging are recalled because the firm's Chapter 11 filing left it unable to monitor its quality program. 26,992 blister packs are affected.

    Product
    Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose]
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 (Devices)·Z-2443-2025·2025-09-03

    Phantom Essential loupe kits recalled because nickel nose pads may cause allergy

    Orascoptic Phantom Essential Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 74 kits are affected.

    Product
    Orascoptic Superior Visualization Phantom Essential kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (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 (Devices)·Z-2445-2025·2025-09-03

    Phantom nose pad kits recalled because nickel content may cause allergic reaction

    Orascoptic Phantom Nose Pad Accessory Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 22 kits are affected.

    Product
    Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose pad and screw) 1 pk. and 20 pk.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V570000·2025-09-03

    Ducati Motorcycles Recalled for Defective Rear Wheel Axle

    Ducati is recalling certain 2018-2025 motorcycles because the rear wheel axle may lose structural integrity and break during riding, risking loss of control. Dealers will replace the axle free of charge.

    Product
    DUCATI — DUCATI STREETFIGHTER, STREETFIGHTER V2, PANIGALE V4 S, STREETFIGHTER V4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0533-2025·2025-09-03

    Three seed baking mix recalled because label omits sesame and other ingredients

    Baker's Authority Three Seed Mix in 5 lb bags is recalled because the label does not list ingredients, including the major food allergen sesame. Millet and flax are also undeclared. 78 units are affected.

    Product
    Baker's Authority Three Seed Mix; 5lb bag; stored dry at room temperature; packaged in silver bag
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-2341-2025·2025-09-03

    OEC 9800 C-arm systems recalled over missing collimator cover lead tape

    GE HealthCare OEC 9800 C-arm systems are recalled because impacted units are missing the full layer of lead tape in the collimator covers, slightly increasing radiation exposure.

    Product
    GE HealthCare OEC 9800.
    Category
    Medical Device
    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·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 W990, T680, T880
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V567000·2025-08-29

    MCI Recalls Electric Buses Due to Battery Overheating and Fire Risk

    Motor Coach Industries is recalling specific 2020-2025 electric buses because an inadequate weld and software error may cause battery overheating and fire.

    Product
    MCI — MCI D45CRTELE, J4500E, D45CRTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V562000·2025-08-29

    Altec utility vehicle cable entry steps can detach during use

    Altec is recalling certain 2011-2025 Aerial Device, Digger Derrick and Service Body vehicles because the cable step wire rope assembly may be improperly secured, allowing the entry step to detach.

    Product
    ALTEC — ALTEC, TEREX DIGGER DERRICK, SERVICE BODY, AERIAL DEVICE, AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V560000·2025-08-29

    Fontaine Recalls 2025-2026 Forklift Trailers Due to Brake System Defect

    Fontaine Trailer Company is recalling 2025-2026 forklift trailers because misinstalled cables may disable the anti-lock brake system, increasing crash risk.

    Product
    FONTAINE — FONTAINE FORKLIFT TRAILER HCIFL12SAT, FORKLIFT TRAILER HCIFL82CTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V566000·2025-08-29

    New Flyer Recalls Electric Buses Due to Battery Overheating Risk

    New Flyer is recalling specific electric bus models because an inadequate weld and software error may cause battery modules to overheat, increasing the risk of fire.

    Product
    NEW FLYER — NEW FLYER XE40, XHE40, XE35, XE60
    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