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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27301–27325 of 114590

  • SevereFDA (Food)·F-0137-2023·2022-11-16

    Vegan Drumsticks Recalled Due to Undeclared Egg Allergen

    DA CHENG VEGETARIAN FOOD INC. is recalling Vegan Drumsticks because they contain egg that is not declared on the label. The product poses a risk to consumers with egg allergies.

    Product
    Vegan Drumsticks, 6.6 lb. bags. Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper Spice, Vegan Seasoning Keep Frozen
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0147-2023·2022-11-16

    Whole Foods Market dipping caramel recalled for undeclared wheat allergen

    Whole Foods Market Dipping Caramel (PLU 34888) is recalled because it contains wheat that was not declared on the label. Consumers with wheat allergies should not consume this product.

    Product
    Whole Foods Market Dipping Caramel, PLU 34888 sold by the pound and packaged in nonflexible plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0148-2023·2022-11-16

    ReadyMeals Chicken Salad Quad Recalled for Undisclosed Tree Nut Allergen

    ReadyMeals Chicken Salad Quad products distributed in CO, NE, NM, SD, and WY have labels missing tree nut (cashew) allergen information. Consumers with tree nut allergies should not consume this product.

    Product
    ReadyMeals Chicken Salad Quad, 12 oz., in a clear plastic container with four compartments, UPC 2 1352 40000 0, Distributed by: Safeway Inc., Pleasanton, CA 94588. Perishable - Keep Refrigerated
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0226-2023·2022-11-16

    Medical Device Procedure Kits Recalled for Foreign Body Reaction Risk

    Boston Scientific recalls ORISE ProKnife Procedure Kits due to higher incidence of foreign body reactions to remnant gel post-procedure, which have required surgical intervention in affected patients.

    Product
    ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0225-2023·2022-11-16

    ORISE Gel Syringe Recall Due to Foreign Body Reaction Risk

    Boston Scientific has recalled ORISE Gel Syringe kits used in gastrointestinal endoscopy due to higher incidence of foreign body reactions from remnant gel requiring surgical intervention.

    Product
    ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0139-2023·2022-11-16

    Vegan Golden Nuggets recalled for undeclared egg allergen

    DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets due to undeclared egg allergen. The product is marketed as vegan but contains egg, which is not declared on the label.

    Product
    Vegan Golden Nuggets, (1 lb. bags) Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper, Vegan Chicken Flavor Seasoning (Food Additive: Modified Starch Seasoning, Yeast Extract (Yeast Extract, Salt, Water), Crisp Powder, Bread…
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0223-2023·2022-11-16

    Neonatal Endotracheal Tube Grip with Detachable Metal Clips Recalled

    CooperSurgical is recalling NEO-fit Neonatal Endotracheal Tube Grips due to metal clips that can become loose or detach. Eleven complaints include three cases of clip ingestion, three removals from the mouth, and one throat laceration.

    Product
    NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0146-2023·2022-11-16

    Hammond's Salted Caramel Cookies Recalled for Undeclared Peanut Allergen

    Hammond's Salted Caramel Cookies contain an undeclared peanut allergen due to mispacking of Peanut Butter Chocolate Chip Cookies into Salted Caramel boxes. Nationwide distribution affected.

    Product
    Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735 Washington St, Denver, CO 80216. Cookies are packaged in sealed, opaque, white, plastic bag, which is packed inside printed on cardstock box. There are 8 boxes…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0138-2023·2022-11-16

    Vegan Golden Nuggets recalled for undeclared egg allergen

    DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets for containing undeclared egg. The product was distributed to restaurants and retail stores in Utah, Virginia, Texas, and California.

    Product
    Vegan Golden Nuggets, (6.6 lb bags) Ingredients: (NON GMO) Textured Soybean Fiber, Isolated Soy Protein, Soybean Oil, Sugar, Salt, Pepper, Vegan Chicken Flavor Seasoning (Food Additive: Modified Starch Seasoning, Yeast Extract (Yeast Extract, Salt, Water), Crisp Powder, Bread…
    Category
    Food
    Distribution
    4 states
  • SevereUSDA FSIS·042-2022·2022-11-16

    Tyson Recalls Raw Ground Beef Due to Foreign Matter Contamination

    Tyson Fresh Meats is recalling raw ground beef products in Texas that may contain reflective mirror-like material. No illnesses have been reported.

    Product
    Tyson Fresh Meats, Inc. — Tyson Fresh Meats, Inc. Recalls Raw Ground Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0136-2023·2022-11-16

    Bombolo Biscotti Italian Cookies Recalled for Undeclared Walnut Allergen

    Sotto i Trulli is recalling Bombolo Biscotti Assorted Italian Cookies due to undeclared walnut allergen. Consumers with walnut allergies should not consume this product.

    Product
    Bombolo Biscotti, Assorted Italian Cookies, Net WT. 16 oz (454g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0224-2023·2022-11-16

    Medical Device Recall: ORISE Gel Submucosal Lifting Agent Due to Foreign Body Reactions

    Boston Scientific is recalling ORISE Gel Submucosal Lifting Agent due to higher incidence of foreign body reactions to retained gel. These reactions caused mass formations requiring surgical intervention.

    Product
    ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device Packaged…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0149-2023·2022-11-16

    Chicken Salad Sandwich Club 18 Inch Tray Recalled for Undisclosed Cashew Allergen

    Albertsons Companies LLC is recalling Chicken Salad Sandwich Club trays because labels fail to disclose tree nuts (cashews) in the ingredient and contains statements. Consumers with cashew allergies may unknowingly consume these sandwiches.

    Product
    Chicken Salad Sandwich Club 18 Inch Tray, Black tray with 16 pre-made sandwiches, UPC 2 9615 90000 0, Distributed by: Safeway Inc., Pleasanton, CA 94588. Perishable - Keep Refrigerated.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0135-2023·2022-11-16

    H-E-B Meal Simple Tomato Basil Soup recalled for undeclared milk allergen

    Bakkavor USA is recalling H-E-B Meal Simple Tomato Basil Soup due to an undeclared milk allergen that poses a risk to consumers with milk allergies.

    Product
    H-E-B Meal Simple Tomato Basil Soup 32 oz. Plastic containers, 6 containers per case Keep Refrigerated.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0189-2023·2022-11-16

    Cardinal Health Insulated Gel Pack Recalled for Infant Safety

    Cardinal Health is recalling its insulated gel pack because it should not be used on infants or neonates. The product labeling will be updated with a caution statement.

    Product
    Cardinal Health INSULATED GEL PACK REUSABLE, SMALL, Cat. 80204A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0194-2023·2022-11-16

    Insulin Pump Cybersecurity Vulnerability Allows Unauthorized Remote Access

    MiniMed 600 series insulin pumps have a cybersecurity vulnerability that could allow unauthorized access, potentially resulting in delivery of too much or too little insulin. Users should disable the Remote Bolus feature.

    Product
    Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711, MMT-1712, MMT-1751, MMT-1752
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Devices)·Z-0222-2023·2022-11-16

    X-Guide X-Mark Probe Tool Recall: Missing Weld Creates Aspiration Risk

    X-NAV Technologies is recalling the X-Guide X-Mark Probe Tool because a critical weld may be missing, potentially allowing the probe tip to detach and fall into a patient's mouth during use, creating a risk of aspiration or swallowing.

    Product
    X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0143-2023·2022-11-16

    BabyBel Snacker Cheese Recall: Undeclared Milk and Almond Allergens

    Taylor Farms Retail is recalling BabyBel Snacker cheese products due to undeclared milk and almond allergens on the ingredient label. Consumers with allergies to these ingredients should not consume the product.

    Product
    BabyBel Snacker (FG0401 SW Snacker ACABB 5pk) Crunch Pak 5.75 oz In sealed plastic tray, 5 trays per case UPC: 732313001572 Keep refrigerated Crunch Pak Item Number - FG0401
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0178-2023·2022-11-16

    La Rosa Brand Pasteurized Crabmeat Recalled for Defective Seal

    RIVER CITY SEAFOOD INTERNATIONAL LLC is recalling 51 cases of La Rosa Brand BluCrab Pasteurized Crabmeat (lot #0531, best by 11/2023) due to defective seals that could allow contamination.

    Product
    La Rosa Brand BluCrab Pasteurized Crabmeat (Jumbo, Lump, Claw) Peso Neto: 454g Can label art is the same for all cans, there is a sticker for each category (Jumbo, Lump, Claw) that goes on the lid.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0183-2023·2022-11-16

    Zio AT Ambulatory ECG Monitoring System Documentation Labeling Update

    iRhythm Technologies is recalling clinical reference materials for the Zio AT cardiac monitoring system due to labeling deficiencies that may delay notification of arrhythmias to healthcare providers. Transmission limits could prevent critical cardiac event reporting.

    Product
    Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio Ambulatory ECG monitoring system
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-0191-2023·2022-11-16

    Cardinal Health insulated gel pack recalled for infant contraindication

    Cardinal Health is recalling approximately 414,194 units of its insulated gel pack because the product should not be used on infants or neonates. The company will update product labeling with a clear warning.

    Product
    Cardinal Health INSULATED GEL PACK REUSABLE, EXTRA LARGE, Cat. 80600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2023·2022-11-16

    Scalpel and StatLock in HydroPICC kits expire before label indicates

    Access Vascular recalls 79 HydroPICC catheter kits because included scalpel and StatLock components have earlier expiration dates than stated on the package.

    Product
    Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0188-2023·2022-11-16

    Cardinal Health Insulated Gel Pack recalled; not safe for infants

    Cardinal Health is recalling 1,209,260 INSULATED GEL PACK REUSABLE, LARGE units because the product is not safe for infants or neonates. The company is adding a warning label.

    Product
    Cardinal Health INSULATED GEL PACK REUSABLE, LARGE, Cat. 80104
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0184-2023·2022-11-16

    FERNO POWER X1 ambulance cot batteries pose fire and burn risk

    Ferno-Washington is recalling 1,922 FERNO POWER X1 ambulance cots with 36V Li-Ion batteries that may become unstable and pose a fire or burn injury risk if dropped, power washed, or abused.

    Product
    FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend Stair Chair Powertraxx (Item #0731403/UDI-DI 00190790004064) not included in this action).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0186-2023·2022-11-16

    Cardinal Health Reusable Gel Pack Contraindicated for Infants and Neonates

    Cardinal Health is recalling 409,738 reusable gel pack units because they should not be used on infants or neonates. The company is adding a caution statement to labeling.

    Product
    Cardinal Health GEL PACK REUSABLE, SMALL, Cat. 70204
    Category
    Medical Device
    Distribution
    Distributed nationwide