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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

13751–13775 of 36679

  • SevereFDA (Devices)·Z-1768-2019·2019-07-24

    CareFusion Recalls Alaris Pump Model 8100 Due to Bezel Plastic Weakening

    CareFusion is recalling Alaris Pump Model 8100 units manufactured between April 2011 and June 2017 because the bezel plastic may weaken, potentially causing infusion errors.

    Product
    Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following products are affected by this recall as they are pumps or pump assemblies with bezels manufactured between April 2011 and June 2017 with the FR-110 plastic.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1556-2019·2019-07-24

    Weaver Popcorn Recalls Cheddar Popcorn Due to Salmonella Concern

    Weaver Popcorn Co. is recalling specific lots of cheddar popcorn due to a concern of possible Salmonella contamination.

    Product
    Cheddar popcorn, bulk, packaged in metalized film, Net Wt. 4.85 lbs., Item No. 107065
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1942-2019·2019-07-24

    Datascope CS100 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS100 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than the minimum run time of operating power.

    Product
    CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V544000·2019-07-24

    Toyota and Lexus Recall Vehicles for Brake Booster Pump Failure

    Toyota is recalling specific 2019-2020 hybrid and luxury vehicles because a brake booster pump failure may disable stability control and braking assist.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4 HYBRID, UX HYBRID, LC500, PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1563-2019·2019-07-24

    ADM Recalls Bulk Gold Medal Flour Due to Potential E. coli O26

    ADM is recalling 191,000 pounds of bulk Gold Medal Flour due to potential E. coli O26. The product was distributed to commercial bakeries and food service locations.

    Product
    Gold Medal Flour Product Code: 805046 Bulk flour
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1564-2019·2019-07-24

    Recall of Pillsbury Hi Gluten Flour due to E. coli risk

    ADM is recalling Pillsbury Hi Gluten Flour because of potential E. coli O26 contamination. The affected flour was distributed to food service in New York and Pennsylvania.

    Product
    Pillsbury BALANCER HI GLUTEN FLOUR BLEACHED BROMATED ENRICHED 50 LB bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1939-2019·2019-07-24

    Datascope Cardiosave Hybrid Intra-Aortic Balloon Pump Recalled for Labeling Defects

    Datascope Corp. is recalling 6,197 Cardiosave Hybrid Intra-Aortic Balloon Pumps worldwide due to inadequate labeling regarding battery maintenance.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1978-2019·2019-07-24

    CooperSurgical Recalls Advincula Delineator Uterine Manipulator Due to Potential Cracking

    CooperSurgical is recalling 213 units of the Advincula Delineator Uterine Manipulator because the soft cup may crack during use, posing a risk of lacerations.

    Product
    Advincula Delineator with Ultem Plastic Soft Cup size 3.0 cm; Part No. AD750SC-KE30 The Advincula Delineator Uterine Manipulator is a single-use disposable device designed specifically for Total Laparoscopic Hysterectomy (TLH), Laparoscopic Assisted Vaginal Hysterectomy…
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1557-2019·2019-07-24

    Commercial Creamery Recalls White Cheddar Cheese Blend Due to Salmonella Risk

    Commercial Creamery Company of Idaho is recalling White Cheddar 5906-KD because it may be contaminated with Salmonella. The product was distributed in Iowa and Indiana.

    Product
    White Cheddar 5906-KD is a non-GMO White Cheddar Cheese Blend dried cheese powder. Product was shipped in bulk bags, net wt 50 lbs. The product label is read in parts: "***WHITE CHEDDAR BLEND 5906KD *** Net Wt. 50 lbs. ***INGREDIENTS: CHEDDAR CHEESE (Pasteurized Milk, Salt…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1578-2019·2019-07-24

    ADM Recalls Bulk Flour Due to Potential E. coli O26 Presence

    ADM is recalling bulk flour products due to the potential presence of E. coli O26. The affected flour was distributed to retailers and commercial bakeries in multiple states.

    Product
    Springup Flr Enr, Mt Bulk Flour Product Code 703020
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·19172·2019-07-24

    Porter-Cable Table Saws Recalled by CPSC Due to Fire Hazard

    Chang Type is recalling Porter-Cable 10-inch table saws sold at Lowe's because the motors can overheat and cause fires. No injuries have been reported.

    Product
    Porter-Cable 10" Table Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1944-2019·2019-07-24

    Datascope CS300 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS300 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than the minimum required operating power.

    Product
    CS300 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3023-55 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1487-2019·2019-07-24

    Pfizer Recalls Milrinone Lactate Injection Bags Due to Sterility Concerns

    Pfizer is recalling specific lots of Milrinone Lactate Injection bags because they may leak, compromising sterility.

    Product
    Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 mL, 100 mL bag, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2776-23, Barcode (01)00304092776233.
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·19V541000·2019-07-23

    BMW Recalls 2019 X5 and X7 Models for Loose Wheel Bolts

    BMW is recalling 2019 X5 xDrive50i and X7 xDrive40i vehicles because left-side wheel bolts may loosen, increasing the risk of a crash.

    Product
    BMW — BMW X7, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·076-2019·2019-07-20

    US Foods Recalls Raw Beef and Pork Due to Possible Contamination

    US Foods is recalling approximately 712 pounds of raw beef and pork products that may be contaminated due to a potential employee injury during production.

    Product
    US Foods Inc. — US Foods Recalls Raw Beef and Pork Products Due to Possible Product Contamination
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·19E046000·2019-07-19

    MORryde Recalls Fifth Wheel Wedge Kits Due to Incorrect Bolts

    MORryde is recalling certain Orbital and You Turn Rubber Pin Box Wedge Kits because incorrect bolt lengths may prevent proper tightening, increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E047000·2019-07-19

    MORryde Recalls Fifth Wheel Pin Boxes Due to Short Bolts

    MORryde is recalling certain You Turn and Orbital Rotating Pin boxes because they may have shorter bolts than required, increasing the risk of a crash.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V538000·2019-07-19

    Hyundai Recalls Genesis G80 and G90 Vehicles for Oil Leak Fire Risk

    Hyundai is recalling 2018 Genesis G80 and 2017-2018 Genesis G90 vehicles because a loose seal may cause oil to leak onto the exhaust manifold, increasing fire risk.

    Product
    GENESIS — GENESIS G90, G80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·075-2019·2019-07-18

    Koch Foods Recalls Breaded Chicken Bites for Undeclared Allergens

    Koch Foods is recalling approximately 743 pounds of breaded chicken bites because they contain undeclared soy, milk, and eggs.

    Product
    Koch Foods — Koch Foods Recalls Breaded Poultry Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1546-2019·2019-07-17

    Baumer Foods Recalls Mislabeled Worcestershire Sauce Sold as Soy Sauce

    Baumer Foods is recalling 10 FL OZ bottles of Worcestershire sauce mislabeled as soy sauce due to an undeclared allergen. The product was distributed to retail locations in six northeastern states.

    Product
    Soy Sauce, 10 FL OZ
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1465-2019·2019-07-17

    Losartan Potassium Tablets Recalled Due to NMBA Impurity Detection

    Golden State Medical Supply Inc. is recalling Losartan Potassium 100 mg tablets because an impurity called NMBA was detected in the active ingredient.

    Product
    Losartan Potassium, 100 mg tablets, 90 count bottle, NDC 60429-318-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1459-2019·2019-07-17

    Macleods Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active ingredient.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1477-2019·2019-07-17

    Methylcobalamin Injection Recalled for Lack of Sterility Assurance

    First Pharma Associates is recalling Methylcobalamin 1 mg/mL Injection vials due to a lack of assurance of sterility.

    Product
    Methylcobalamin 1 mg/mL Injection, 8 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252
    Category
    Drug
    Distribution
    2 states