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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21601–21625 of 26896

  • HighFDA (Devices)·Z-1363-2022·2022-07-20

    PALMAZ GENESIS Transhepatic Biliary Stent Risk of Dislodgement

    Cordis is recalling 1,089 units of PALMAZ GENESIS Transhepatic Biliary Stents due to potential stent dislodgement in two specific device sizes. Affected patients should contact their healthcare provider.

    Product
    PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX, PG3990BPS, PG3990BPX.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1367-2022·2022-07-20

    Anti-SARS-CoV-2 IgG Reagent: Stability Time Overstated in Instructions

    Ortho-Clinical Diagnostics is recalling Anti-SARS-CoV-2 IgG Quantitative Reagent Pack because the Instructions For Use incorrectly state on-analyzer stability of 8 weeks when the actual supported time is 6 weeks.

    Product
    Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿ ECi/ECiQ/3600 Immunodiagnostic Systems and VITROS¿ 5600/XT 7600 Integrated Systems. Product Code: 6199960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1208-2022·2022-07-20

    Hydroxocobalamin Compounded Injections Recalled for Lack of Sterility Assurance

    Tailor Made Compounding is recalling 63 vials of Hydroxocobalamin 25mg/mL injectable solution nationwide due to lack of assurance of sterility. Consumers should not use affected batches.

    Product
    Hydroxocobalamin 25mg/mL, 10mL-vial, Room Temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1228-2022·2022-07-20

    Sermorelin/Glycine Injectable Recalled for Lack of Sterility Assurance

    A compounded sermorelin/glycine injectable has been recalled because the manufacturer cannot assure the product is sterile. The recall affects approximately 2,870 vials distributed nationwide.

    Product
    Sermorelin/Glycine 2000mcg/5mg/mL, 7.5mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1419-2022·2022-07-20

    1st Phorm Protein Bars Recalled for Plastic and Paper Contamination

    Bakery Barn is recalling 1st Phorm Level-1 Bar Chocolate Crunch protein bars due to possible contamination with plastic and paper foreign material. Consumers should not consume the affected product.

    Product
    1st Phorm High Quality Protein Level-1 Bar Chocolate Crunch Protein Bars. 15 Bars Per Box. Net Wt. 12-2.22oz (63g) Bars 33.3oz (945g) Per Box. UPC: 5002619600
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1379-2022·2022-07-20

    Tibial Prosthesis Component Recalled for Intraoperative Screw Loosening Defect

    Tibial prosthesis components may have blind screws that cannot be loosened during surgery, potentially requiring surgical procedure changes and extended operative time.

    Product
    Tibial Component. orthopedic prosthesis. Model Nos: Small, W 16-2817/02 Medium, W 16-2817/05 Large, W 16-2817/07
    Category
    Medical Device
    Distribution
    15 states
  • HighNHTSA·22V513000·2022-07-20

    2022 BMW X3 Fuel Rail Defect May Cause Engine Fire

    BMW is recalling 2022 X3 xDrive30i vehicles because the high-pressure fuel rail may crack and cause a fuel leak in the engine compartment, increasing the risk of fire. Dealers will replace the fuel rail free of charge.

    Product
    BMW — 2022 BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1212-2022·2022-07-20

    Melanotan I Injectable Vials Recalled Due to Lack of Sterility Assurance

    Tailor Made Compounding has recalled 182 vials of Melanotan I injectable due to lack of assurance of sterility. The affected vials were distributed nationwide and in Puerto Rico.

    Product
    Melanotan I 200mcg/mL (2mg/ml), a) 1.5mL-vial, b) 5 mL-vial, Refrigerate, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1377-2022·2022-07-20

    Modular Orthopedic Implant Screws May Not Loosen During Surgery

    FDA recalls certain Endo Model orthopedic implants because the blind screws may not loosen during surgery, potentially requiring surgeons to change their approach and prolonging the procedure.

    Product
    Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No #15-2814/04). orthopedic prosthesis.
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-1359-2022·2022-07-20

    MiniMed 780G Insulin Pump battery cap deterioration may cause power loss

    Medtronic MiniMed is recalling 83,398 MiniMed 780G insulin pumps distributed throughout the United States due to battery cap deterioration that may cause power loss and device malfunction.

    Product
    MiniMed 780G Insulin Pump (O.U.S. Version)
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Drugs)·D-1233-2022·2022-07-20

    Compounded Testosterone/Anastrozole Injectable Vials Recalled for Sterility Assurance

    Tailor Made Compounding is recalling 106 vials of compounded testosterone/anastrozole injectable due to lack of sterility assurance. The product was distributed nationwide in the USA and Puerto Rico.

    Product
    Testosterone Cypionate/Anastrozole 200mg/1mg/mL, a) 4 mL-vial, b)10mL-vial, Room temperature, Tailor Made Compounding
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V512000·2022-07-20

    Alliance RV Paradigm and Valor Travel Trailers Awning Weld Separation

    Alliance RV is recalling 2022-2023 Paradigm and Valor travel trailers due to electric retractable awning weld separation that may allow the awning to drop unexpectedly, increasing injury risk.

    Product
    ALLIANCE RV — 2023 ALLIANCE RV PARADIGM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V509000·2022-07-19

    2022 Kia Sorento and Telluride recalled for spare tire brake defect

    Kia is recalling 2022 Sorento and Telluride vehicles with an incorrect spare tire that can impair the anti-lock braking and traction control systems. These defects increase the risk of a crash.

    Product
    KIA — 2022 KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V507000·2022-07-15

    Arcimoto hybrid electric vehicles high voltage connector latch defect

    Arcimoto is recalling certain 2019-2022 model year hybrid electric vehicles with a high voltage connector defect that may detach, causing sudden loss of power steering and drive power.

    Product
    ARCIMOTO — 2022 ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22185·2022-07-14

    Sakar International Recalls Tony Hawk Silver Helmets Due to Head Injury Risk

    Sakar International is recalling about 12,655 Tony Hawk Silver Metallic multi-purpose helmets sold at Walmart from March to June 2022. The helmets do not meet federal safety standards for positional stability and retention, and may fail to protect in a crash.

    Product
    Tony Hawk Silver Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22758·2022-07-14

    Westfield Outdoor Recalls Outfitter and Big Horn Tents for Smoke Inhalation Hazard

    Westfield Outdoor is recalling approximately 5,050 Cabela's Outfitter and Big Horn camping tents because the stove jack ring can deteriorate under heat and create smoke inside the tent, posing a smoke inhalation risk.

    Product
    Outfitter and Big Horn tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1402-2022·2022-07-13

    Prairie City Bakery Peanut Butter Chocolate Chip Cakes Recalled for Salmonella

    Prairie City Bakery is recalling Peanut Butter Chocolate Chip Ooey Gooey Butter Cakes due to Salmonella contamination from recalled Jif peanut butter ingredient. Products were distributed to gas stations and convenience stores nationwide.

    Product
    Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake 2oz. individual UPC: 7-9788436718-2; 10 individual units per display unit; 6 display units per wholesale case.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1319-2022·2022-07-13

    Palindrome HSI Chronic Catheter Recalled for Potential Hub Leaking

    Covidien is recalling Palindrome HSI Chronic Catheters due to a potential leaking condition in the catheter hub that may cause unanticipated fluid return during dialysis. Approximately 13,526 units distributed worldwide are affected.

    Product
    Palindrome HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1399-2022·2022-07-13

    Giant Eagle Cupcakes Recalled Due to Salmonella Contamination Risk

    Giant Eagle Cupcakes (GE Cupcake 6 Buckeye, 18Oz) recalled due to potential Salmonella contamination from Jiff Peanut Butter. 14 units distributed to Pennsylvania.

    Product
    GE 29765500000 Cupcake 6 Buckeye 18Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1313-2022·2022-07-13

    Palindrome Precision H Chronic Catheter Recalled for Potential Hub Leakage

    Covidien is recalling certain Palindrome Precision H Chronic Catheters because the hub may leak, causing unexpected fluid to flow back during use. This FDA Class I recall affects 26,675 units distributed globally.

    Product
    Palindrome Precision H Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1396-2022·2022-07-13

    Giant Eagle Peanut Butter Fudge Split Cake Recalled for Potential Salmonella

    Giant Eagle's Peanut Butter Fudge Split Cake, made with Jiff Peanut Butter, is being recalled due to potential Salmonella contamination. The recall affects units distributed in Pennsylvania.

    Product
    GE 25115700000 Bakery, Cake, Peanut Butter Fudge Split 25.6 Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1393-2022·2022-07-13

    Giant Eagle Torte Peanut Butter Recalled for Potential Salmonella Contamination

    Giant Eagle Torte Peanut Butter (62 oz, code GE 23984200000) is recalled due to potential Salmonella contamination from the Jiff peanut butter ingredient. Consumers should not consume this product.

    Product
    GE 23984200000 Torte Peanut Butter 62Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1397-2022·2022-07-13

    Giant Eagle Peanut Butter Brownie Recalled for Salmonella Risk

    Giant Eagle is recalling a 16-ounce Peanut Butter Creme Brownie made with Jiff Peanut Butter due to potential Salmonella contamination. The product was distributed to Pennsylvania.

    Product
    GE 25135900000 Bakery, Brownie, Peanut Butter Creme 16Oz
    Category
    Food
    Distribution
    1 state