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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20301–20325 of 39655

  • SevereFDA (Food)·F-2332-2017·2017-06-14

    Krisppee Clam Cake Mix Recalled for Undeclared Milk Allergen

    Krisppee Products Co. is recalling Famous Rhode Island Clam Cake Mix in 5, 25, and 50 lb sizes because it contains undeclared milk.

    Product
    KRISPPE FAMOUS RHODE ISLAND CLAM CAKE MIX NET WEIGHT 5 lbs., 25 lbs., 50 lbs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2270-2017·2017-06-14

    High Liner Foods Breaded Haddock Recalled for Undeclared Milk

    ISF "USA", LLC is recalling High Liner Foods Breaded Haddock Tail Portions due to undeclared milk, a major allergen.

    Product
    High Liner Foods, Breaded Haddock Tail Portions 5 oz.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2259-2017·2017-06-14

    Arrow International Recalls Central Venous Access Kits Due to Needlestick Risk

    Arrow International is recalling 43,394 units of MAC Two-Lumen Central Venous Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R) Access Device, Integral Hemostasis Valve, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 -8 Fr. Catheters. The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2281-2017·2017-06-14

    Arrow VPS Access Kit Recalled Due to Needlestick Injury Risk

    Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters (PICCs) to the goal location which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2268-2017·2017-06-14

    Arrow Pressure Injectable PICC Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling 43,394 units of Pressure Injectable PICC Kits due to safety cover disengagement and needlestick injury reports.

    Product
    Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2017·2017-06-14

    Stryker Recalls Berchtold Chromophare F300 Exam Lights Due to Mounting Defect

    Stryker Communications is recalling 57 Berchtold Chromophare F300 exam lights because a tolerance issue may cause the equipment to fall, posing a risk of serious injury.

    Product
    Berchtold Chromophare F300 Exam Light CHROMOPHARE examination lights are medical lights used for local illumination of the patients' body so that illnesses, injuries and disabilities can be diagnosed and treated
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2279-2017·2017-06-14

    Arrow International Recalls CVC Kits Due to Needlestick Injury Risk

    Arrow International is recalling specific CVC kits because the packaged BD Eclipse Needle may disengage, posing a needlestick injury risk to medical personnel.

    Product
    AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.The ARROWg+ard Blue¿ Catheter permits venous access to the central circulation by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2275-2017·2017-06-14

    Arrow Central Venous Catheter Kits Recalled for Needlestick Injury Risk

    Arrow International is recalling specific central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.

    Product
    Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions requiring central venous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0888-2017·2017-06-14

    MedPark Pharmacy Recalls Methylcobalamin Injection Vials Due to Sterility Concerns

    MedPark Pharmacy is recalling methylcobalamin 1mg/1mL injection vials because the company cannot ensure the product is sterile. The affected lot was distributed to a patient in Maryland.

    Product
    methylcobalamin 1mg/1mL, vial for injection, Rx only, MedPark Pharmacy 2002 Medical Pkwy. # 170 Annapolis, MD 21401
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2278-2017·2017-06-14

    Arrow International Recalls Multi-Lumen CVC Kits Due to Needlestick Risk

    Arrow International is recalling specific multi-lumen central venous catheter kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2287-2017·2017-06-14

    Arrow International Recalls Access Kits Due to Needlestick Injury Risk

    Arrow International is recalling Access Kits with Maximal Barrier Precautions because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    Arrow¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The Arrow¿ GlideThru" Peel-Away Sheath/Dilator Introducer is used for the percutaneous introduction of diagnostic or therapuetic devices into the vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2272-2017·2017-06-14

    Arrow Central Venous Catheter Kits Recalled for Needlestick Injury Risk

    Arrow International is recalling certain central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.

    Product
    Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2289-2017·2017-06-14

    Arrow Access Kit Recalled Due to Needlestick Injury Risk

    Arrow International is recalling specific Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.

    Product
    Arrow¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Central Venous Catheter The Arrow¿ GlideThru" Peel-Away Sheath/Dilator Introducer is used for the percutaneous introduction of diagnostic or therapuetic devices into the vasculature
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2286-2017·2017-06-14

    Arrow PICC Recall Due to Safety Cover Disengagement and Needlestick Risk

    Arrow International is recalling Arrow PICC devices with Chlorag+ard Technology because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.

    Product
    Arrow PICC with Chlorag+ard Technology The ArrowEVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for intravenous therapy, blood sampling…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2334-2017·2017-06-14

    Whole Foods Oatmeal Chocolate Chip Cookies Recalled for Undeclared Walnuts

    Whole Foods Market is recalling Oatmeal Chocolate Chip Cookies due to undeclared walnuts, a major food allergen.

    Product
    Oatmeal Chocolate Chip Cookies, 18pk, NET WT. 0 lb 10 oz (283 g), Dist. by Whole Foods Market, 1105 N. Lamar, Austin, TX 78703 USPC 0247181 004992
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2261-2017·2017-06-14

    Arrow Percutaneous Sheath Introducer Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling Percutaneous Sheath Introducer Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.

    Product
    Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostatis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5-8 Fr. Catheters. The Arrow Percutaneous Sheath Introducer permits venous access and catheter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2273-2017·2017-06-14

    Viking Breaded Flounder Fillets Recalled for Undeclared Milk

    ISF "USA", LLC is recalling Viking Breaded Natural Flounder Fillets due to undeclared milk. The recall affects 263 cases distributed within the United States.

    Product
    Viking, Breaded Natural Flounder Fillets 4 oz.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2331-2017·2017-06-14

    Krisppee Clam Fry Mix Recalled for Undeclared Milk Allergen

    Krisppee Products Co. is recalling Clam Fry Mix in 5, 25, and 50 lb sizes because the product contains undeclared milk.

    Product
    KRISPPE CLAM-FRY-MIX NET WEIGHT 5 lbs., 25 lbs., 50 lbs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2275-2017·2017-06-14

    ISF USA Recalls Raw Breaded Fish Portions for Undeclared Milk

    ISF "USA", LLC is recalling A&W Raw Breaded Fish Portions due to undeclared milk. The recall affects 374 cases distributed within the United States.

    Product
    A&W, GIN 0040995 Raw Breaded Fish Portions 3.5 oz
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·17V380000·2017-06-14

    Piaggio Recalls 2016-2017 Moto Guzzi Motorcycles for Brake Hose Defect

    Piaggio is recalling 2016-2017 Moto Guzzi motorcycles because the front ABS brake hose may rub against the engine, causing a fluid leak that increases crash risk.

    Product
    PIAGGIO — PIAGGIO, MOTO GUZZI V7 III SPECIAL 750, MOTO GUZZI V7 III RACER 7, V9 BOBBER, V7 III STONE 750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2333-2017·2017-06-14

    Krisppee Batter Mix Recalled for Undeclared Milk Allergen

    Krisppee Products Co. is recalling Krisppee Batter Mix for Fish & Chips due to undeclared milk. The product was distributed in Rhode Island and Massachusetts.

    Product
    KRISPPE BATTER MIX For FISH & CHIPS Net WEIGHT 5 lbs., 25 lbs., 50 lbs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2285-2017·2017-06-14

    Arrow PICC Kit Recalled Due to BD Eclipse Needle Safety Cover Issues

    Arrow International is recalling certain PICC kits because the packaged BD Eclipse Needle has a safety cover that may disengage, posing a needlestick injury risk.

    Product
    Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ArrowEVOLUTIONTM Pressure Injectable P1CC with Chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2273-2017·2017-06-14

    Arrow International Recalls Central Venous Catheter Kits Due to Needlestick Risk

    Arrow International is recalling specific central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.

    Product
    Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2300-2017·2017-06-14

    Arrow Arterial Catheterization Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling Arterial Catheterization Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.

    Product
    Arterial Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
    Category
    Medical Device
    Distribution
    Distributed nationwide