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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

8201–8225 of 113896

  • HighFDA (Devices)·Z-2108-2025·2025-07-16

    Alcon Constellation vitrectomy packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2025·2025-07-16

    Nuclear medicine systems may show unintended radial detector motion during scans

    Varicam, Millennium VG, Millennium VG Hawkeye and Discovery VH nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software version. 21 units affected.

    Product
    Varicam, Millennium VG, Millennium VG Hawkeye, Discovery VH Nuclear Medicine System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2097-2025·2025-07-16

    Infinia nuclear medicine systems may show unintended radial detector motion

    Infinia, Infinia Hawkeye, Infinia II and Infinia II Hawkeye 4 nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software. 1,822 units affected.

    Product
    Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye 4 Nuclear Medicine system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2109-2025·2025-07-16

    Alcon Constellation procedure packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Combined Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 89,495 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Combined Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2105-2025·2025-07-16

    VersaCross transseptal sheath kits may have a punctured sterile barrier pouch

    VersaCross Transseptal Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS 63CM/45DEG/D0 SHEATH VXS2112 VERSACROSS SHEATH (63CM 45DEG D0)-J Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, includ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0278-2025·2025-07-16

    Wegmans semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Wegmans Semi-Sweet Chocolate Nonpareils are being recalled because of undeclared milk. 595 cases are affected across nine states and the District of Columbia.

    Product
    Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ (1 LB 2.5 OZ) (524 g), packaged in a plastic tub and packed 12 per case, Distributed by: Wegmans Food Markets, Inc. Rochester, NY 14603. Ingredients: Sugar, Chocolate Liquor, Cacao Fat, Corn Starch, Soy Lecithin (emulsifier
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2110-2025·2025-07-16

    Alcon Custom Pak surgical kits may have damaged lidding compromising sterility

    Alcon Custom Paks, customer-designed sterile surgical kits, are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 15,557 kits affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience kits intende
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2025·2025-07-16

    VersaCross access kits may have a hole in the sterile pouch

    VersaCross Access Solution kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF WIRE 63CM/45DEG/D1) VXSK0102 VXSK (180J RF WIRE 63CM/55DEG/D0) VXSK0103 VXSK (180P RF WIRE 63CM/45DEG/D0) VXSK0121 VXSK (180P RF WIRE 63CM/45DEG/D1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0220-2025·2025-07-16

    Wegmans chocolate chip mini muffins may contain foreign objects of metal

    Wegmans brand Chocolate Chip Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; CHOCOLATE CHIP; NET WT 13.5 OZ; packaged in plastic clamshell; UPC 7789053223
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2104-2025·2025-07-16

    VersaCross RF wire lots may have a punctured sterile barrier pouch

    The VersaCross RF Wire is being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units are affected.

    Product
    VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device approved and commercialized in Japan only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0219-2025·2025-07-16

    Wegmans French toast mini muffins may contain foreign objects of metal

    Wegmans brand French Toast Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    a. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 22 OZ (1 LB 6 OZ) 624 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789058612 b. Wegmans brand Mini Muffins; FRENCH TOAST; NET WT 13 OZ (369 g); packaged in plastic clamshell; UPC: 7789052435
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0320-2025·2025-07-16

    Crown Point shelled edamame recalled because the label does not declare soy

    Crown Point Shelled Edamame in 22 lb cases is being recalled because the label declares shelled edamame but does not specify or declare soy. 1,046 cases are affected.

    Product
    Crown Point Shelled Edamame, net wt. 22lbs. UPC 813973 01840 4. Product is packaged in carton box with poly liner. Distributed by Alpine Foods Distributing Inc. Milwaukie, OR. Product of China.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2106-2025·2025-07-16

    Torflex transseptal guiding sheath kits may have a punctured sterile pouch

    Torflex Transseptal Guiding Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atri
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0258-2025·2025-07-16

    Ghouribeh date rolls recalled over undeclared wheat, soy and sesame

    C Sweet Ghouribeh Rolls with date, sesame and pistachios are being recalled because wheat, soy and sesame are undeclared. 30 units are affected.

    Product
    C Sweet Ghouribeh Rolls with date, sesame, & pistachios 10 oz., UPC 642896991132
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0218-2025·2025-07-16

    Wegmans blueberry mini muffins may contain foreign objects of metal origin

    Wegmans brand Blueberry Mini Muffins family pack is being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; Blueberry; NET WT 20 OZ (1 LB 4 OZ) 567 g; FAMILY PACK; packaged in plastic clamshell; UPC 7789053227
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-2090-2025·2025-07-16

    TrueDent Clear dental resin cartridges carry an expiration date formatting error

    TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.

    Product
    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0234-2025·2025-07-16

    Organic red and green cabbage recalled over reach truck fluid contamination

    Organic red and green cabbage is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. WLD HRVST OG2 RED CABBAGE 2. USA/MX OG2 RED CABBAGE 3. USA ORGC GRN CABBAGE 4. WLD HRVST OG2 GREEN CABBAGE
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0222-2025·2025-07-16

    Red Delicious, Gala and organic apples recalled over reach truck fluid

    A range of apples, including Red Delicious, Gala, Granny Smith and Fuji, is being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.

    Product
    1. USA APLS RED DEL TOTE 2. USA APLE RED DEL 80CT 3. DOMESTIC APPLE GALA TOTES 4. USA APPLES GALA 80CT 5. WLD HRVST OG2 WAXF GRNY SMTH 6. WLD HRVST OG2 WAXF FUJI 7. WLD HRVST OG2 WAXF GALA 8. WLD HRVST OG2 WAXF PINK LADY 9. WA OG1 HNYC
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0223-2025·2025-07-16

    Organic and conventional carrots recalled over possible reach truck fluid contamination

    A range of carrot products is being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. BLTHSFRSH CARROT CRINKLE 2. OG2 RNBW BNCH CRTS 3. OG2 GRN TOP CARRO 4. ORGC JUMBO CARRO 5. OG2 CARROTS BAG 6. OG2 CARROTS BAG 7. OG2 CARROTS BAG 8. WLD HRVST OG2 CELLO CARROTS 9. OG1 PETITE CARROT 10. USA OG1 BBY PLD CARRT 11. WLD HRVST OG2 BBY
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0229-2025·2025-07-16

    Kale bunches recalled over possible contamination with reach truck fluid

    Kale bunches, including organic and lacinato kale, are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.

    Product
    1. USA KALE BUNCH CTN 2. USA OG2 KALE 3. USA OG1 LACINATO KALE
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0515-2025·2025-07-16

    In Your Face tinted mineral sunscreen recalled over manufacturing practice deviations

    In Your Face Mineral Tint SPF 31 tinted sunscreen is being recalled because of cGMP deviations. 76 bottles are affected.

    Product
    In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingredients, Biodegradable & Baby Safe, 50 mL - 1.7 fl oz per bottle, Manufactured for IN YOUR FACE Skin Care, Belleair Bluffs, FL, Made in USA, NDC: 73369-1601-1
    Category
    Drug
    Distribution
    3 states