The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

13776–13800 of 53086

  • HighFDA (Devices)·Z-1310-2023·2023-04-05

    Iradimed MRidium MRI Infusion Pump Syringe Adapter Sets Recalled for Occlusion Risk

    Iradimed is recalling MRidium MRI 1000 Series Infusion Set Syringe Adapter Sets due to a defective part that can limit venting function and cause occlusion, potentially interrupting medication delivery.

    Product
    Iradimed Corporation MRidium MRI 1000 Series Infusion Sets, MRI Infusuui Set - Syringe Adapter Set, REF 1057-50,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2023·2023-04-05

    CoCr Femoral Head hip implant compatibility removed due to motion limitations

    Zimmer is updating the compatibility matrix for the CoCr Femoral Head XS hip implant to remove pairing with Epsilon Durasul Constrained Acetabular Liners due to insufficient range of motion in flexion/extension.

    Product
    CoCr Femoral Head, XS, 38/-8, Taper 12/14-Intended to be used as a modular head component for articulation in total hip arthroplasty. Item Number: 01.01012.384
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0681-2023·2023-04-05

    Seasoned Green Laver Recalled for Undeclared Soy, Wheat, Fish, and Sesame

    Lemonland Food Corp is recalling Seasoned Green Laver sold in Washington due to undeclared allergens including soybean, wheat, fish (anchovy), and sesame seeds. Consumers with allergies to these ingredients should not consume this product.

    Product
    Seasoned Green Laver distributed in un-labeled plastic containers 8oz. and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0667-2023·2023-04-05

    Seasoned Perilla Leaves Recalled Due to Undeclared Allergens

    Lemonland Food Corp recalled Seasoned Perilla Leaves in 6oz, 8oz, and 12oz containers distributed in Washington because the product contains undeclared allergens: sesame, soy, wheat, fish, and shrimp.

    Product
    Seasoned Perilla Leaves distributed in un-labeled plastic containers 6oz, 8oz, and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0481-2023·2023-04-05

    FDA Recalls Glimepiride Tablets Due to Manufacturing Quality Violations

    Direct Rx is voluntarily recalling Glimepiride 2 mg tablets nationwide due to manufacturing practice violations. The recall affects multiple lot numbers of 30-count and 90-count bottles distributed across the United States.

    Product
    Glimepiride, USP, 2 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0488-30; b) 90-count bottle, NDC 61919-0448-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0652-2023·2023-04-05

    Rold Gold Original Tiny Twists Pretzels Recalled for Undeclared Soy

    Frito-Lay is recalling Rold Gold Original Classic Tiny Twists Pretzels because the product contains undeclared soy lecithin, which may affect consumers with soy allergies.

    Product
    Rold Gold Original Classic Tiny Twists Pretzels in 16oz UPC 2840004768 packaged in a flexible bag
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0682-2023·2023-04-05

    Hot Pepper in Soy Sauce Recalled for Undeclared Soy and Wheat

    Lemonland Food Corp recalled Hot Pepper in Soy Sauce distributed in 12-ounce containers due to undeclared soybean and wheat allergens. Consumers with soy or wheat allergies should not consume this product.

    Product
    Hot Pepper in Soy Sauce distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0672-2023·2023-04-05

    Seasoned Garlic Stem Recalled Due to Undeclared Fish and Sesame Allergens

    Lemonland Food Corp recalled Seasoned Garlic Stem products due to undeclared fish (anchovy) and sesame allergens. Affected products were distributed in Washington from February 16-23, 2023.

    Product
    Seasoned Garlic Stem distributed in un-labeled plastic containers 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0659-2023·2023-04-05

    Spicy Cucumber Salad recalled for undeclared sesame, fish, and wheat allergens

    Lemonland Food Corp recalls Spicy Cucumber Salad due to undeclared sesame seeds, fish (anchovy), and wheat allergens. The product was distributed in multiple container sizes in Washington.

    Product
    Spicy Cucumber Salad distributed in un-labeled plastic containers 8oz, 12oz. and 16oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0663-2023·2023-04-05

    Seasoned Hot Pepper Leaves recalled for undeclared fish and sesame allergens

    Lemonland Food Corp recalls Seasoned Hot Pepper Leaves from Washington due to undeclared Fish (Anchovy) and Sesame Seeds allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Seasoned Hot Pepper Leaves distributed in un-labeled plastic containers 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0665-2023·2023-04-05

    Stir-Fried Kimchi Recalled for Undeclared Allergens: Fish, Shrimp, Wheat, Sesame

    Lemonland Food Corp recalls 12 oz. containers of Stir-Fried Kimchi distributed in Washington due to undeclared allergens: fish (anchovy), shrimp, wheat, and sesame. Consumers with allergies to these ingredients should not consume this product.

    Product
    Stir-Fried Kimchi distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1291-2023·2023-04-05

    Alcon Custom Pak Surgical Procedure Packs Recalled for Incomplete Seals

    Alcon Research is recalling 1,035 Custom Pak Surgical Procedure Packs with incomplete seals that affect sterility. These packs were distributed to surgical facilities in 14 US states.

    Product
    Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Description: 17533-04 DR GROSS LPS LLC 18704-03 CATARACT SURGI CARE 18382-03 DR GEORGE ZAMBELLI BEAVER VALLEY ASC 8685-21 CATARACT PACK EYE SURGICAL CNTR OF AR 19451-02 DR ROESKE PACK INLAND VALLEY SURGERY CTR…
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-0689-2023·2023-04-05

    Mary's Gone Crackers recalled for potential foreign material contamination

    Mary's Gone Crackers Super Seed Seaweed & Black Sesame Crackers may contain foreign material. Approximately 2,376 cases were distributed throughout the USA.

    Product
    Mary s Gone Crackers Super Seed Seaweed & Black Sesame Crackers Product Item number: 10033380101 UPC: 8 53665 00510 7
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1303-2023·2023-04-05

    Express Mini 500 Chest Drain Recalled for Inadequate Instructions

    The Express Mini 500 Dry Seal Chest Drain has been recalled because its instructions do not adequately warn against draining it for continued use or using it outside healthcare settings. Approximately 8,184 cases were distributed worldwide.

    Product
    Express Mini 500 Dry Seal Chest Drain, Part Number 16400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V240000·2023-04-05

    MCI Recalls 2019-2021 Coaches Due to Obstructed Rear Lighting

    Motor Coach Industries is recalling 2019-2021 J4500, D45CRTLE, and J3500 coaches because rear lighting may be obstructed by bike racks, increasing crash risk.

    Product
    MCI — MCI D45CRTLE, J4500, J3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0664-2023·2023-04-05

    Seasoned Vegetables Recalled for Undeclared Soy and Wheat Allergens

    Lemonland Food Corp is recalling Seasoned Vegetables (Cirsium Setidens) distributed in Washington due to undeclared soy and wheat allergens. Consumers with soy or wheat allergies should not consume this product.

    Product
    Seasoned Vegetables (Cirsium Setidens) distributed in un-labeled plastic containers 6oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0662-2023·2023-04-05

    Seasoned Korean Lettuce Recalled for Undeclared Fish Allergen

    Lemonland Food Corp recalled Seasoned Korean Lettuce distributed in Washington due to undeclared fish (anchovy). Consumers with fish allergies should not consume this product.

    Product
    Seasoned Korean Lettuce distributed in un-labeled plastic containers 6oz or 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0688-2023·2023-04-05

    Danncy Vainilla Pure Mexican Vanilla Extract Contains Prohibited Coumarin

    Danncy Vainilla Pure Mexican Vanilla Extract is being recalled because the product contains coumarin, a prohibited substance. Consumers should stop using the product.

    Product
    Danncy Vainilla Pure Mexican Vanilla Extract Clear Gluten Free Produced by Juan Miguel Anzaldua Gutierrez NET 33.8 FL OZ (1.0L) UPC 7503000781137 packaged in clear plastic bottles and Danncy Vainilla Pure Mexican Vanilla Extract Gluten Free Produced by Juan Miguel Anzaldua…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1306-2023·2023-04-05

    FDA recalls ACL ELITE refurbished analyzer to remove Anti-Xa test

    Instrumentation Laboratory recalled ACL ELITE refurbished coagulation analyzers to remove the HemosIL Liquid Anti-Xa test definition.

    Product
    ACL ELITE Refurbished-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or fibrinolysis testing. Part Number: 0000880311R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0685-2023·2023-04-05

    Stainless Steel Water Bottles Recalled for Lead Leaching from Welded Screw Cap

    BINDLE BOTTLE is recalling Stainless Steel Water Bottles because the cup's screw cap is attached by a weld that leaches lead into drinking water.

    Product
    Stainless Steel Water Bottle The product comes in four sizes: 32 oz., 24 oz., 20 oz., and 13 oz.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V238000·2023-04-04

    Tie rod fastener defect in commercial trucks risks steering failure

    Daimler Trucks is recalling commercial vehicles with a tie rod that may be missing a fastener, allowing the steer arm to detach and causing potential loss of steering control.

    Product
    FCCC — FCCC, FREIGHTLINER, WESTERN STAR MT50E, 114SD, M2, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V237000·2023-04-04

    Freightliner and FCCC trucks recalled for windshield wiper linkage failure

    Daimler Trucks North America is recalling certain 2020-2022 Freightliner and FCCC trucks due to windshield wiper linkage failure that can reduce visibility. Dealers will inspect and replace affected parts free of charge.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC M2, S2C, S2RV, S2G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E030000·2023-04-04

    Cummins Recalls Onan Generator Sets Due to Fuel Hose Fire Risk

    Cummins is recalling certain Onan QG 2800i generator sets because a fuel hose may not be properly secured, creating a gas leak and fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E028000·2023-03-31

    Felling Trailers Recall Warn Winch Remotes Due to Water Intrusion Risk

    Felling Trailers is recalling 2022-2023 trailers equipped with Warn winches because water may enter the remote control, causing corrosion and unintentional winch operation.

    Product
    FELLING — FELLING DECK-OVER, DROP-DECK
    Category
    Vehicle
    Distribution
    Distributed nationwide