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 deaths or serious injuries are reported, 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.

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10651–10675 of 31360

  • HighNHTSA·23V439000·2024-11-06

    2023 Lincoln Nautilus Brake System Risk from Defective Rear Shock Absorbers

    Ford is recalling 366 2023 Lincoln Nautilus vehicles due to incorrectly manufactured rear shock absorbers that may damage the brake hose, potentially extending stopping distance and increasing crash risk. Dealers will inspect and replace affected components at no cost.

    Product
    LINCOLN — 2023 LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0027-2025·2024-11-06

    Cinacalcet tablets recalled for nitroso impurity above FDA limits

    Dr. Reddy's Laboratories is recalling Cinacalcet 60 mg tablets nationwide because testing detected N-nitroso impurity exceeding FDA interim limits. The recall affects 35,880 bottles.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0245-2025·2024-11-06

    Codman Surgical Patties and Strips recalled for elevated endotoxin levels

    Integra LifeSciences has recalled Codman Surgical Patties and Strips (Model 801407) due to higher-than-expected endotoxin levels in raw materials, resulting in out-of-specification endotoxin in finished products used in brain surgery.

    Product
    SURG PAT XRAY 1/2X3 Model/Catalog Number: 801407. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0257-2025·2024-11-06

    Covidien Chameleon PTA Balloon Catheter Recalled for Failed Pressure Testing

    Covidien is recalling specific lots of its Chameleon PTA Balloon Catheter that failed in-house pressure testing. The affected catheters were distributed worldwide to the US and 18 countries.

    Product
    Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm x 75cm (CFN CH05-40-75US), 6mm x 40mm x 75cm (CFN CH06-40-75US), 7mm x 40mm x 75cm (CFN CH07-40-75US), 8mm x 40mm x 75cm (CFN CH08-40-75US), 9mm x 40mm x 75cm (CFN CH09-40-75US), 10mm x 40mm x 75cm (CFN CH10-40-75US),
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0255-2025·2024-11-06

    Surgical Patties and Strips Recalled for Higher Endotoxin Levels

    Integra LifeSciences is recalling Surgical Patties and Strips (Model 801456) due to higher-than-expected endotoxin levels in raw materials. These surgical devices are used for tissue protection during surgery, including CNS procedures.

    Product
    SURG STRP 3X6 Model/Catalog Number: 801456. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0140-2025·2024-11-06

    GE Healthcare Giraffe infant incubator recalled for formaldehyde exposure

    GE Healthcare Giraffe Omnibed infant incubators may release airborne formaldehyde when newly manufactured. Customers were notified in June 2023 to run units for one week to reduce potential off-gassing.

    Product
    GE Healthcare Giraffe Omnibed Carestation CS1, combination infant incubator and infant warmer. Model Numbers: 1) 2082844-001-01040418; 2) 2082844-001-01046784; 3) 2082844-001-01052324; 4) 2082844-001-01052572; 5) 2082844-001-01055337; 6) 2082844-001-01065693; 7) 2
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0093-2025·2024-11-06

    Home Chef Chicken Street Taco Kits Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Home Chef Chicken Street Taco Kits due to Listeria monocytogenes contamination in the cooked chicken. The kits were distributed across 32 states with use-by dates from September through November 2024.

    Product
    Item 406581, UPC 40134 30435, Home Chef Kit Street Taco Chicken With Tray, 2/4.985 LB. Distributed by Fresh Creative Foods, Vista, CA or by Reser's Fine Foods Inc. Beaverton, OR. Item 406581, UPC 40134 30435, Home Chef Chicken Street Taco Kit With Trays, 2/4.985 LB. Distributed
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0072-2025·2024-11-06

    New Horizen BBQ Chicken Sandwich Recalled for Listeria Contamination

    Whitsons Food Service recalls 1,152 units of New Horizen Gourmet BBQ Pulled Chicken Sandwiches distributed in New York due to potential Listeria monocytogenes contamination.

    Product
    New Horizen Gourmet BBQ Pulled Chicken Sandwich on Everything Bialy; KEEP FROZEN; COOK & SERVE; Cooking Instructions: Conventional oven (Preheat oven to 350oF). Thaw product overnight. Cook meal for 20 mins or until an internal temp of 165oF. For quality purposes only, cook produ
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0094-2025·2024-11-06

    Home Chef Asian Style Chicken Stir Fry Kits Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Home Chef Asian Style Chicken Stir Fry meal kits due to potential Listeria monocytogenes contamination in the cooked chicken. The affected products were distributed across 30 states.

    Product
    Item 406873, UPC 40134 30852, Home Chef Asian Style Chicken Stir Fry OP With Trays 2/6.5 LB. Distributed by Fresh Creative Foods, Vista, CA.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0083-2025·2024-11-06

    Don Pancho Chicken Quesadilla Meal Kits Recalled for Listeria Monocytogenes

    Reser's Fine Foods is recalling Don Pancho Chicken Quesadilla Express Meal Kits due to potential Listeria monocytogenes contamination in the cooked chicken component. No illnesses have been reported.

    Product
    Item 404852, UPC 71117 12507, Don Pancho Chicken Quesadilla Express Meal Kit. Make 3 Quesadilla. Ready in 4 MIN. Net wt. 22.5 oz (1 LB 6.5 OZ) 638g. Case GTIN 10071117125075, Case UPC 7111712507, Don Pancho Chicken Quesadilla Express Meal Kit. 6/22.5oz bags. Distributed by Re
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-0275-2025·2024-11-06

    King LTSD Oropharyngeal Airway Recalled for Uncleared Pediatric Indication

    King Systems is recalling the King LTSD Size 2 oropharyngeal airway because it was distributed with a pediatric indication that lacks proper FDA 510(k) clearance, exceeding exemption limits.

    Product
    KING LTSD,SIZE 2, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KLTSD432
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0273-2025·2024-11-06

    King LTSD Oropharyngeal Airway Recalled for Unauthorized Pediatric Use

    King Systems' KING LTSD oropharyngeal airway was marketed for pediatric use but lacked the required FDA clearance for that indication. Approximately 17,925 units were distributed nationwide.

    Product
    KING LTSD,SIZE 0, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KLTSD430
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0281-2025·2024-11-06

    Smith & Nephew Knee Prosthesis Component Packaging Error: Wrong Implant Shipped

    Smith & Nephew is recalling a knee prosthesis component after discovering some packages contained a different implant than labeled. No illnesses or injuries have been reported.

    Product
    smith&nephew GENESIS II NONPOROUS POSTERIOR STABILIZED FEMORAL COMPONENT, SIZE 5 LEFT, REF 71421015; Uncoated knee femur prosthesis, metallic
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0258-2025·2024-11-06

    17-OH Progesterone ELISA Kit Recalled for Labeling Discrepancy

    DRG International is recalling 504 units of its 17-OH Progesterone ELISA kit (Model EIA-1292) due to mismatched control acceptance ranges between the Certificate of Analysis and component labels, causing test failure.

    Product
    17-OH Progesterone ELISA 96 well kit- An enzyme immunoassay for the quantitative in vitro diagnostic measurement of 17-OH Progesterone (17-OHP) in serum or plasma Model/Catalog Number: EIA-1292
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0276-2025·2024-11-06

    KING LTSD Oropharyngeal Airway Kit Recalled for Unapproved Pediatric Use

    King Systems Corp. is recalling KING LTSD airway kits (Model KKLTSD4325) because they were marketed for pediatric use without FDA approval for that indication. Approximately 36,727 units were distributed nationwide.

    Product
    KING LTSD,SIZE 2.5, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KKLTSD4325
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0260-2025·2024-11-06

    Surgical tracking device patient labels show incorrect expiration date

    Patient label stickers on Insight Base Flex tracking device snaps have incorrect expiration dates. The stickers show manufacturing date instead of actual expiration date, though the correct date appears on carton and pouch labels.

    Product
    Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that includes reflective features that facilitate imaging of the (attached) instrument using instrument tracking technology when used with a compatible tracking system. Each TrackX¿ Snap has a
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Food)·F-0070-2025·2024-11-06

    International Delight Peppermint Mocha Mislabeled as Zero Sugar Product Recall

    DANONE US LLC is recalling Home Alone International Delight Peppermint Mocha Zero Sugar beverages because the product is labeled as zero sugar but actually contains sugar. The recall affects 1,799 cases distributed across multiple states.

    Product
    Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.
    Category
    Food
    Distribution
    13 states
  • HighNHTSA·24V260000·2024-11-04

    2022-2024 Tiffin Motorhomes Cooktop Circuit Board Fire Risk

    Tiffin Motorhomes is recalling certain 2022-2024 Allegro RED 360 and related motorhomes because the LED backlight circuit board in the cooktop may overheat, increasing fire risk. No fires or injuries have been reported.

    Product
    TIFFIN — 2022 TIFFIN ALLEGRO RED 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V193000·2024-11-03

    Autocar Xpeditor Fuse Box Short Circuit from Water Intrusion

    Autocar is recalling 2020-2022 Xpeditor vehicles whose external fuse box may short circuit from water intrusion, causing unexpected stall and increasing crash risk. Dealers will mount the box vertically and install a protective shield.

    Product
    AUTOCAR — 2022 AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V191000·2024-11-03

    2020-2022 Jeep Wrangler Frame Stud Fuel Tank Puncture Recall

    Chrysler recalls 2020-2022 Jeep Wranglers because a frame stud may puncture the fuel tank during a crash, increasing fire risk. Approximately 35,829 vehicles are affected.

    Product
    JEEP — 2022 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V120000·2024-11-02

    2022–2024 International and IC Bus Trucks/Buses: Engine Control Software Defect

    Navistar is recalling 2022-2024 International HV and MV trucks and 2022-2023 IC Bus TC buses. An engine control module software defect can cause the engine to override the parking brake when the transmission remains in drive or reverse and the power take-off switch is engaged, resulting in unintended vehicle movement.

    Product
    INTERNATIONAL — 2022 INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V118000·2024-11-02

    2022-2023 BMW M3 Door Locking Software Defect Recall

    BMW is recalling certain 2022-2023 models due to a door locking software defect. Faulty ECU programming may prevent doors from locking while driving, increasing crash injury risk.

    Product
    BMW — 2023 BMW M3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V119000·2024-11-02

    International commercial trucks recalled for park brake software defect

    Navistar is recalling 2018-2022 International trucks with a software defect that may prevent the park brake from holding during power-take-off operation, risking unexpected vehicle movement.

    Product
    INTERNATIONAL — 2022 INTERNATIONAL HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V115000·2024-11-02

    2021-2023 Dodge Durango Recalled for Misaligned Rear Spoiler Detachment Risk

    Chrysler is recalling 2021-2023 Dodge Durango vehicles because the rear spoiler may not be properly aligned with the roof. The misaligned spoiler can be damaged during liftgate use and potentially detach, becoming a road hazard.

    Product
    DODGE — 2021 DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V113000·2024-11-02

    2015–2023 Thor Motor Coach Palazzo Front Brackets May Detach While Driving

    Thor Motor Coach is recalling 1,969 Palazzo recreational vehicles from model years 2015–2023 because front brackets supporting the fiberglass panel may become loose and detach while driving, creating a road hazard.

    Product
    THOR MOTOR COACH — 2017 THOR MOTOR COACH PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide