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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11501–11525 of 36636

  • SevereNHTSA·20V168000·2020-03-20

    Terex Recalls 2009-2016 Aerial Devices Due to Lift Cylinder Defect

    Terex is recalling 2009-2016 TCX and SML aerial devices because lift cylinder rod eyes may fail, causing the boom to drift down and increasing injury risk.

    Product
    TEREX — TEREX TCX, SML
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V171000·2020-03-20

    Newmar Recalls Motorhomes Due to Insufficiently Tightened Brake Caliper Bolts

    Newmar is recalling specific 2019-2020 motorhomes because brake caliper mounting bolts may be loose, which can reduce braking effectiveness and increase crash risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, VENTANA, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V158000·2020-03-19

    Forest River Recalls Vans Due to Transmission Shifter Cable Separation

    Forest River is recalling 2016-2020 vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.

    Product
    LONE STAR HANDICAP VANS — LONE STAR HANDICAP VANS, FOREST RIVER, COACHMEN L1 VAN, REV, ORION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V170000·2020-03-19

    Husqvarna 701 Motorcycles Recalled for Fuel Leak Fire Risk

    KTM is recalling 2018-2020 Husqvarna Vitpilen and Svartpilen 701 motorcycles because fuel may leak from the pump area, increasing fire risk.

    Product
    HUSQVARNA — HUSQVARNA VITPILEN 701, SVARTPILEN 701
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V161000·2020-03-19

    Forest River Recalls 2019-2020 Motorhomes Due to Brake Caliper Bolt Issue

    Forest River is recalling 2019-2020 Berkshire and Sportscoach motorhomes because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, SPORTSCOACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V159000·2020-03-19

    Tremcar Recalls 2018-2020 Semi-Trailers Due to Brake Washer Fracture Risk

    Tremcar is recalling 2018-2020 406 and 407 semi-trailers because brake actuator washers may fracture, potentially reducing braking ability and increasing crash risk.

    Product
    TREMCAR — TREMCAR 407 SEMI-TRAILER, 406 SEMI-TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V164000·2020-03-19

    BMW Recalls 2020 Models for Front Seat Belt Sensor Defect

    BMW is recalling 2020 models because front seat belt sensors may misread occupants, causing improper airbag and pretensioner deployment.

    Product
    BMW — BMW M850I, M340I, X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V165000·2020-03-19

    BMW Recalls 2020 R 1250 RT and GS Motorcycles for Driveline Defect

    BMW is recalling 2020 R 1250 RT and GS motorcycles because a damaged pivot pin may loosen the final drive connection, increasing crash risk.

    Product
    BMW — BMW R 1250 RT, R 1250 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0829-2020·2020-03-18

    Shearer's Yellow Tortilla Chips Recalled for Undeclared Milk

    Shearer's Snacks is recalling specific lots of Yellow tortilla chips due to undeclared milk. The product was shipped to two distributors and is fully accounted for.

    Product
    Shearer's Yellow tortilla chips, round Mini and Restaurant sizes, packaged in clear film pillow bags in the following weights: 1oz (100 count per case), 1.5oz (72 count per case), 2oz (60 count per case), and a bulk case16oz bags (10 count per case)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1442-2020·2020-03-18

    CME BodyGuard Microset Infusion Sets Recalled for Fluid Under-Delivery

    CME America is recalling BodyGuard Microset infusion sets because they may under-deliver fluids when used with specific infusion pump systems.

    Product
    BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The BodyGuard Infusion Pump System is designed to transfer medication and fluids intravenously.
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Food)·F-0832-2020·2020-03-18

    Chocolate Dairy Powder Recalled Due to Potential Metal Fragment Contamination

    International Food Products Corporation is recalling 21 bags of chocolate dairy powder because an ingredient may have been contaminated with metal fragments.

    Product
    Profile Food Ingredients, 10# Choc Dairy Pwd PFI-1010, packaged in 50 lb bags.
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·20V154000·2020-03-18

    Bentley Recalls Bentayga Vehicles Due to Third-Row Seat Belt Defect

    Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1476-2020·2020-03-18

    Qiagen Rotor-Gene Q Software Recall for Incorrect Concentration Reporting

    Qiagen is recalling Rotor-Gene Q instruments with software version 2.3.4 because a bug causes concentration results to be reported as logarithmic values, potentially leading to false negative test results.

    Product
    QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time detection of PCR assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1003-2020·2020-03-18

    American Health Packaging Recalls Ranitidine Tablets Due to NDMA Levels

    American Health Packaging is recalling 53,619 cartons of Ranitidine Tablets, 150 mg, due to potential N-Nitrosodimethylamine (NDMA) amounts above FDA-established levels.

    Product
    Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC carton: 60687-322-01; NDC Unit Dose Card: 60687-322-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1010-2020·2020-03-18

    Redline Pharmacy Recalls Vancomycin Injectable Due to Processing Control Deficiencies

    Redline Pharmacy Solutions is recalling 3 doses of Vancomycin 900MG Injectable due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Vancomycin 900MG in 100ML 0.9% NACL Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1007-2020·2020-03-18

    Redline Pharmacy Recalls Morphine Sulfate Due to Processing Control Deficiencies

    Redline Pharmacy Solutions is recalling Morphine Sulfate 20 mg/mL intrathecal syringes due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Morphine Sulfate, 20 mg/mL intrathecal, 20 mL per syringe. Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1004-2020·2020-03-18

    Precision Dose Recalls Ranitidine Oral Solution Due to NDMA Impurity

    Precision Dose Inc. is recalling Ranitidine Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit Dose Cups per case, NDC: 68094-204-61; Unit Dose Cup NDC: 68094-204-59], Rx only, Precision Dose, Inc., South Beloit, IL 61080
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0817-2020·2020-03-18

    Tova Industries Recalls American Bounty Chili Mix Due to Metal Shavings

    Tova Industries is recalling American Bounty Chili Mix w/Beans because of possible metal shavings in an ingredient. The recall covers 225 cases distributed to 11 states and the UAE.

    Product
    American Bounty brand Chili Mix w/Beans, Item #46628, in 20.8 oz. metallic pouches, 6 pouches per case.
    Category
    Food
    Distribution
    11 states