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.

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19851–19875 of 90011

  • HighNHTSA·23V317000·2023-05-04

    Ferrara Recalls 2022 Fire Trucks Due to Winch Remote Water Intrusion

    Ferrara Fire Apparatus is recalling 2022 Ultra and Inferno fire trucks because water in the winch remote can cause corrosion and unintentional operation.

    Product
    FERRARA — FERRARA ULTRA, INFERNO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V319000·2023-05-04

    PJ Trailers Coupler May Loosen and Separate, Posing Crash Risk

    PJ Trailers is recalling certain 2022-2024 trailers with Demco EZ Latch Gooseneck Couplers because the mounting bolts may loosen, causing the coupler to separate and creating a crash risk.

    Product
    PJ TRAILERS — PJ TRAILERS LD, LS, LX, LY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V324000·2023-05-04

    2022-2023 Land Rover Range Rover Second-Row Armrest Latch Failure Recall

    Jaguar Land Rover is recalling 2022-2023 Range Rover vehicles because the second-row armrest latch may fail, allowing unsecured objects to strike occupants during a crash. Dealers will replace the locking arm free of charge.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23C004000·2023-05-04

    Baby Trend Recalls Hybrid 3-in-1 Booster Seats Due to Latch Webbing Fraying

    Baby Trend is recalling approximately 2,600 Hybrid 3-in-1 Combination Booster Seats because the latch assembly webbing may fray, potentially failing to restrain a child in a crash.

    Product
    CHILD SEAT:LATCH STRAP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V325000·2023-05-04

    Entegra and Jayco Class B RVs Recalled: Fuel Hose Clamp Defect

    Jayco, Inc. is recalling certain 2021-2024 Class B recreational vehicles. A fuel hose clamp may be inadequate, potentially causing gasoline leaks and increasing fire risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ETHOS, SWIFT, SOLSTICE, EXPANSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0802-2023·2023-05-03

    Savor Imports IQF Raspberries recalled for potential Hepatitis A contamination

    Savor Imports IQF Whole Raspberries (Lot 20220210) are recalled nationwide due to potential Hepatitis A contamination. Consumers should not eat the product and should return or discard it.

    Product
    Savor Imports IQF Whole Raspberries; Net Wt 2-5lb; MFG# 341798; UPC: 10684476003771
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V314000·2023-05-03

    Bentley Recalls Flying Spur Vehicles Due to Screen Bracket Defect

    Bentley is recalling 2021-2023 Flying Spur vehicles because an incorrectly installed rear entertainment screen bracket could become a projectile in a crash, increasing injury risk.

    Product
    BENTLEY — BENTLEY FLYING SPUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0749-2023·2023-05-03

    Lamb Weston Frozen Hash Brown Patties Recalled for Undeclared Wheat

    Lamb Weston Sales is recalling frozen hash brown patties due to undeclared wheat allergen. The recall affects approximately 1605 cases distributed to foodservice customers across multiple states and international locations.

    Product
    G5300 Lamb's Supreme Hash Brown Patties, Frozen, 24 patties packed in blank unlabeled tray, 12 trays packaged in one case. Net Wt. 33.75LB (15.30kg). UPC 1 00 44979 75300 7. The ingredients statement read: POTATOES, VEGETABLE OIL (CONTAINS OR OR MORE OF THE FOLLOWING: CANOLA…
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0755-2023·2023-05-03

    Premium Makoto Honey Ginger Salad Kit Recalled for Listeria Contamination

    Fresh Express is recalling Premium Makoto Honey Ginger Salad Kits distributed in five states because the product tested positive for Listeria monocytogenes. Consumers should not consume this product.

    Product
    PREMIUM MAKOTO HONEY GINGER SALAD KIT TOTAL NET WT 8.75 OZ (248g) DRESSING 2.03 FL OZ (60 mL) SALAD & TOPPING 6.5 OZ (184g) DISTRIBUTED BY PUBLIX SUPER MARKETS, INC., LAKELAND, FL 33802 UPC 0 41415 18386 5
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0753-2023·2023-05-03

    Fresh EXPRESS Lettuce Salad Kit Recalled for Listeria

    Fresh EXPRESS Chopped Kit Caesar Romaine Lettuce has been recalled due to testing positive for Listeria monocytogenes. The affected product was distributed to Florida, Georgia, North Carolina, South Carolina, and Virginia.

    Product
    Fresh EXPRESS Chopped Kit Caesar Romaine Lettuce TOTAL NET WT. 9.4 OZ (266g) SALAD & TOPPINGS: NET WT. 6.9 OZ (196g) DRESSING 2.5 fl. oz. (74 mL)/NET WT 2.5 oz. (71g) fresh express incorporated P.O. BOX 80599, SALINAS, CA 93912 UPC 0 71279 30919 4
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0754-2023·2023-05-03

    Fresh Express Chopped Kit Recalled for Listeria monocytogenes

    Fresh Express Chopped Kit Chipotle Cheddar salad has been recalled because it tested positive for Listeria monocytogenes. The product was distributed to Florida, Georgia, North Carolina, South Carolina, and Virginia.

    Product
    Fresh Express Chopped Kit Chipotle Cheddar TOTAL NET WT. 11.3 oz (320G) SALAD TOPPINGS NET WT 9.1 oz (258Gg) DRESSING 2.3 fl. oz. (68 mL)/NET WT 2.2oz (62g) FRESH EXPRESS INCORPORATED P.O. BOX 80599, SALINAS, CA 93912 UPC 0 71279 30604 9
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0760-2023·2023-05-03

    Patagonia Foods Blackberries Recalled for Possible Hepatitis A

    Patagonia Foods is recalling frozen blackberries (Lot 20422) distributed in six U.S. states due to possible Hepatitis A contamination. Consumers should not consume the product.

    Product
    Patagonia Foods 3610100 Blackberry IQF Product of Mexico Net Wt. 30 LBS. (13.61 kg) Production/Lot Code 20422 Distributed By: Patagonia Foods, LLC. San Luis Obispo, CA 93401 patagoniafoods.com
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1472-2023·2023-05-03

    Draeger Infinity M300 Patient Monitor Software Displays Inaccurate ECG Readings

    Draeger Infinity M300/M300+ patient monitoring systems may display or print ECG waveforms with inaccurate QRS amplitudes due to software peaks being dropped on narrow waveforms.

    Product
    Draeger Infinity M300 and M300+, for use with the ICS to monitor ECG and pulse oximetry on ambulatory and non-ambulatory adult and pediatric patients using wireless communication over the Infinity patient monitoring network,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1466-2023·2023-05-03

    Stryker ORTHOLOC 3Di Fusion Plate Contains Incorrect Laser Markings

    Wright Medical Technology recalls Stryker ORTHOLOC 3Di Fusion Plate MTP Right devices due to incorrect dorsiflexion descriptions laser marked on the parts. 41 units distributed nationwide.

    Product
    stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1425-2023·2023-05-03

    Surgical forceps may fail to open during endoscopic procedures

    Richard Wolf surgical forceps may fail to open when the endoscope shaft is bent. Affected units distributed worldwide; users should check lot numbers and discontinue use if affected.

    Product
    FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0752-2023·2023-05-03

    Enriched Hot Dog Buns Recalled for Undeclared Sesame Allergen

    Our Family White Hot Dog Enriched Buns are being recalled due to undeclared sesame. The recall affects approximately 28,700 units distributed in Michigan, Ohio, Indiana, and Illinois, and poses a risk to consumers with sesame allergies.

    Product
    Our Family White Hot Dog Enriched Buns, 8 count 12oz. retail unit UPC 0-70253-75107-3
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1468-2023·2023-05-03

    Mani Trocar Kits Recalled for Packaging Defect Compromising Sterility

    Mani Trocar Kits (Models MTK23S and MTK25S) are being recalled due to a packaging defect that may compromise the sterile barrier. The recall affects 45 kits distributed to one consignee in Missouri.

    Product
    Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar with the valved cannula and 1 pc. infusion cannula.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1436-2023·2023-05-03

    Sterile surgical C-section kit light handle covers recalled for separation risk

    ROi CPS LLC recalls sterile surgical C-section kits due to light handle covers that may separate and fall during use. The recall affects 1,312 kits distributed in Florida and Missouri.

    Product
    Sterile surgical convenience kit: regard Item Number 800706005, LD0091E - OH C-Section Pack.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1423-2023·2023-05-03

    Biopsy forceps may fail to open when endoscope is bent

    Biopsy forceps may become unable to open when the endoscope shaft is bent approximately 90 degrees. Additional bending of the forceps shaft can prevent opening entirely.

    Product
    FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0554-2023·2023-05-03

    Tadalafil Tablets Recalled Due to Manufacturing Practice Violations

    Northwind Pharmaceuticals is recalling 23 bottles of Tadalafil 5 mg tablets nationwide due to manufacturing process deviations. The FDA classified this as a Class II recall.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0569-2023·2023-05-03

    Fyremadel Ganirelix Acetate Injection Recalled for Glass Contamination

    Sun Pharmaceutical is recalling 24,194 prefilled syringes of Fyremadel (ganirelix acetate) injection due to glass contamination found in a unit from lot HAD1190A. The recall affects units distributed nationwide with expiration 02/2024.

    Product
    FYREMADEL — FYREMADEL (GANIRELIX ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0769-2023·2023-05-03

    Popped water lily seeds recalled due to undeclared milk

    Karma Spices and Trading Company is recalling Karma White Cheddar Cheese Popped Water Lily Seeds because the product contains undeclared milk. The recall affects 1,423 units distributed in Michigan and online.

    Product
    Karma White Cheddar Cheese Popped Water Lily Seeds packed in 1.5oz pouches UPC: 617201892589
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·23V315000·2023-05-03

    Capacity Recalls 2022 TJ Series Trucks Due to Missing Seat Clip

    Capacity of Texas is recalling 2022 TJ 5000, 6500, and 9000 trucks because a missing safety clip on the passenger jump seat could allow it to fall, increasing injury risk.

    Product
    CAPACITY — CAPACITY TJ 9000, TJ 6500, TJ 5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1421-2023·2023-05-03

    Carefusion Vaginal Specula Recalled for Incorrect Labeling and Packaging

    Carefusion recalled 726 units of two vaginal specula models with labels and laser etchings switched during packaging. This mislabeling could result in use of an unintended product.

    Product
    (1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2) Carefusion V. Mueller Pederson Vaginal Specula, Catalog #GL31, Medium, 4 x 7/8" (10.2 x 2.2cm).
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-1467-2023·2023-05-03

    Stryker ORTHOLOC 3Di Fusion Plate Recalled for Incorrect Marked Descriptions

    Wright Medical Technology is recalling Stryker ORTHOLOC 3Di Fusion Plate MTP Right surgical implants due to incorrect dorsiflexion descriptions laser marked on 50 units distributed nationwide.

    Product
    stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
    Category
    Medical Device
    Distribution
    Distributed nationwide