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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20876–20900 of 27460

  • HighFDA (Devices)·Z-0050-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kits Recalled Due to Incorrect Expiration Dates

    Freeman Pancreatic Flexi-Stent Kits are recalled due to device labels displaying incorrect expiration dates that extend shelf life. Affected units were distributed in the US and select countries from March 2018 to September 2020.

    Product
    Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catalog Number: 6503
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0074-2023·2022-10-19

    Yellowfin Tuna Round Steaks Recalled for Elevated Histamine Levels

    Worldwide Seafood Products LLC is recalling Tidal Seafood Yellowfin Tuna Round Steaks due to elevated histamine levels. The affected product was distributed to California, Texas, and New Mexico.

    Product
    Tidal Seafood Yellowfin Tuna Round Steaks 7 oz MED and LG Best Buy 6/17/2024 & 6/20/2024
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0026-2023·2022-10-19

    Medical device retrieval basket labels show incorrect expiration dates

    Hobbs Medical recalls the Helical Retrieval Basket due to labels displaying incorrect expiration dates that extend the device's shelf life. Affected units distributed worldwide from March 2018 to September 2020 may be used beyond their validated lifespan.

    Product
    Hobbs Helical Retrieval Basket Catalog Number: 4806
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0035-2023·2022-10-19

    Ready Meals crab legs product recalled for undeclared fish allergen

    Albertsons Companies is recalling Ready Meals Snow Crab Legs Imitation Surimi in Oregon and Washington due to undeclared fish (anchovy) allergen. Consumers with fish allergies should not consume this product.

    Product
    Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ CAL 300 NET WT. 0lb 12oz (340g) ready2eat Ingredients: Fish Protein (one or more Pollock, Pacific Whiting), Water, Lemon, Tomato Paste, What Starch, High Fructose Corn Syrup, Sugar, Egg Whites, Sorbitol, Crabmeat (Chi
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0033-2023·2022-10-19

    Eden Organic Apple Juice Recalled for Excessive Patulin

    Eden Foods is recalling Eden Organic Apple Juice in multiple sizes because excessive levels of patulin, a mycotoxin from rotted apples, were found in certain lots. Rotted apples were not removed during processing.

    Product
    Eden Organic Apple Juice in 32floz., 64floz., and 1.82L sizes, all sizes in glass bottle. Glass bottles packed 12, 32floz. bottles per wholesale case and 6, 64floz. / 1.82L bottles per wholesale case. 32floz. UPC code: 0 0024182 00067 2 32floz. GTIN case code: 1 0024182 00067 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0064-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels that extend perceived shelf life beyond actual device longevity.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6582
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0058-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Distributed with Incorrect Expiration Date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on the device labels. Affected units distributed in the US and internationally from March 2018 to September 2020 may have been used beyond their actual safe shelf life.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6544
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0035-2023·2022-10-19

    Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Dates

    Hobbs Medical Grasping Forceps (Catalog 5008) were distributed with incorrect expiration dates that extend shelf life beyond the device's actual safe use period. Affected units with lot numbers ending in 'R' were distributed from March 2018 to September 2020.

    Product
    Hobbs Medical Grasping Forceps Catalog Number: 5008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0009-2023·2022-10-19

    Skincell Mole & Skin Corrector Serum Recalled Due to Unapproved Drug Status

    Justified Laboratories is recalling Skincell Mole & Skin Corrector Serum because it was marketed without FDA approval. The affected product was distributed throughout the United States, Puerto Rico, and Canada.

    Product
    Skincell Mole & Skin Corrector Serum, 1 fl. oz./30 mL jars, Distributed By: Justified Laboratoires, Arlington, TX 76011 USA UPC 8 10077 53221 8
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0061-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates

    Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0042-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kit Label Bears Incorrect Expiration Date

    Hobbs Medical is recalling Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual product expiration, potentially resulting in use of expired devices.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0034-2023·2022-10-19

    Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Date Labeling

    Hobbs Medical, Inc. is recalling Grasping Forceps due to incorrect expiration dates on device labels. Affected devices may be used beyond their safe shelf life if the mislabeled expiration dates are not corrected.

    Product
    Hobbs Medical Grasping Forceps Catalog Number:5004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0047-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit Recall: Incorrect Expiration Date Label

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent Kits with incorrect expiration dates on labels, potentially allowing devices to be used beyond their actual safe shelf life. Affected units were distributed from March 2018 to September 2020.

    Product
    Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0055-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recalled for Incorrect Expiration Date

    Hobbs Medical recalled Freeman Pancreatic Flexi-Stents due to incorrect expiration dates on device labels. The mislabeled dates extend shelf life, potentially allowing use of expired devices.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6533
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0022-2023·2022-10-19

    Hobbs Posi-Stop Injection Needle Recall - Incorrect Expiration Date

    Hobbs Medical is recalling Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend shelf life. Devices distributed between March 2018 and September 2020 could be used beyond their actual expiration.

    Product
    Hobbs Posi-Stop Injection Needle Catalog Number: 4712
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0016-2023·2022-10-19

    Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling Polypectomy Snare devices (Catalog Number 4564) due to incorrect expiration dates on labels that extend the stated shelf life. The 35 affected units, distributed in the US and select countries, may be used beyond their actual safe shelf life.

    Product
    Hobbs Medical Polypectomy Snare Catalog Number: 4564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0076-2023·2022-10-19

    Frozen Yellowfin Tuna Poke Recalled for Potential Elevated Histamine Levels

    Worldwide Seafood Products LLC is recalling 40 cases of Tidal Seafood Yellowfin Tuna Poke (Best Buy 6/18/2024) distributed to California, Texas, and New Mexico due to potential elevated histamine levels in the frozen tuna.

    Product
    Tidal Seafood Yellowfin Tuna Poke Best Buy 6/18/2024
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0087-2023·2022-10-19

    PET/CT imaging system loses vital signs data in strong Wi-Fi environments

    Certain PET/CT imaging systems may lose vital sign monitoring due to Wi-Fi interference, potentially requiring patient rescans.

    Product
    Positron Emission Tomography and Computed Tomography System, Model: uMI 550
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0013-2023·2022-10-19

    Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Dates

    Hobbs Medical is recalling its Cytology Brush (catalog 4204) because device labels show incorrect expiration dates that extend the claimed shelf life. Affected devices were distributed in the US and several other countries from March 2018 to September 2020.

    Product
    Hobbs Medical Cytology Brush Catalog Number: 4204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0010-2023·2022-10-19

    Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling Spray Catheter devices due to incorrectly labeled expiration dates that extend shelf life beyond the actual safe-use period. The recall affects 275 units distributed between March 2018 and September 2020.

    Product
    Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0066-2023·2022-10-19

    Freeman Pancreatic Stent Recall: Incorrect Expiration Date on Device Labels

    Freeman Pancreatic Flexi-Stents with incorrect expiration dates on labels may be used beyond their validated shelf life. The recall affects devices distributed in the US and five other countries from March 2018 through September 2020.

    Product
    Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0081-2023·2022-10-19

    Prismaflex M Set Recall for Mistranslated Weight Restriction Instructions

    Baxter Healthcare is recalling Prismaflex M Sets (524,376 devices nationwide) due to a mistranslation in instructions for use that provides contradictory patient body weight restrictions for renal replacement therapy.

    Product
    Prismaflex M Set: M60 (product code 106696), M100 (product code 106697). For use in providing continuous fluid management and renal replacement therapies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0040-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits Recalled for Incorrect Expiration Date Labels

    Hobbs Medical is recalling Biliary Pigtail Stent Kits for incorrect expiration dates on product labels that may extend shelf life. Affected kits were distributed nationwide and internationally between March 2018 and September 2020.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0037-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration dates

    Hobbs Medical is recalling certain Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual validity. Affected devices distributed between March 2018 and September 2020 may be used beyond their true expiration date.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0017-2023·2022-10-19

    Hobbs Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling transbronchial aspiration needles with incorrect expiration dates on labels. The 18 affected units were distributed in the US, Canada, Austria, Belgium, Finland, and Norway from March 2018 to September 2020.

    Product
    Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
    Category
    Medical Device
    Distribution
    Distributed nationwide