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

Category

Minimum severity

Clear filters

13701–13725 of 36668

  • SevereFDA (Drugs)·D-1498-2019·2019-07-31

    Pharma-Natural Recalls Double Tussin DM Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.

    Product
    DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg, Guaifenesin 300 mg) in each 5ml teaspoon, 4 FL OZ (120 mL) bottle, Distributed by: Pamby Dist., Miami, FL 33414, NDC 63708-121-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2058-2019·2019-07-31

    Zyno Medical Administration Sets Recalled Due to Inverted Pinch Clamp Defect

    Zyno Medical LLC is recalling administration sets with inverted pinch clamps that may cause blood to be drawn from patients instead of delivering fluid.

    Product
    Zyno Medical Administration Set -105"ADMIN SET 20DP, W/2 Y SITE, CVCLMPS- For Use with Zyno Medical Infusion pumps or Gravity Feed Product Code:B2-70072
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1526-2019·2019-07-31

    Gericare Geri-Tussin DM Recalled for Potential Microbial Contamination

    Geritrex, LLC is recalling Gericare Geri-Tussin DM due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2081-2019·2019-07-31

    GammaPod Stereotactic Radiotherapy System Recalled for Alignment Drift

    Xcision Medical Systems is recalling two GammaPod Stereotactic Radiotherapy Systems because a loose bolt caused alignment drift and reduced radiation dose output.

    Product
    GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving…
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1520-2019·2019-07-31

    Geritrex Recalls Diphenhydramine Oral Liquid Due to Potential Microbial Contamination

    Geritrex, LLC is recalling 8,645 bottles of Diphenhydramine Oral Liquid due to cGMP deviations that may result in microbial contamination.

    Product
    Diphenhydramine Oral Liquid Alcohol Free, 12.5 mg/5 mL, 4 fl oz (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-204-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1965-2019·2019-07-31

    Probar Meal Superfood Slam Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,908 Superfood Slam meal bars nationwide and in Canada due to undeclared milk and soy allergens.

    Product
    PROBAR MEAL Superfood Slam, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1582-2019·2019-07-31

    Brand Castle Recalls Grinch Sugar Cookie Mix Due to E. coli Risk

    Brand Castle LLC is recalling The Grinch Sugar Cookie Mix with Sprinkles because a supplier reported potential E. coli contamination in the flour used.

    Product
    The Grinch Sugar Cookie Mix with Sprinkles, 22.3 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • SevereUSDA FSIS·080-2019·2019-07-27

    Premium Foods USA Recalls Siluriformes Fish Products Lacking Import Inspection

    Premium Foods USA is recalling 121,151 pounds of Siluriformes fish products imported from ineligible countries without required inspection.

    Product
    Premium Foods USA, Inc., Recalls Siluriformes Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·19V557000·2019-07-26

    Temsa Recalls 2014-2019 TS45 Buses for Steering Hose Defect

    Temsa is recalling 2014-2019 TS45 buses because hydraulic steering hoses may leak or burst, potentially affecting steering ability and increasing crash risk.

    Product
    TEMSA — TEMSA TS45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·079-2019·2019-07-26

    Kent Quality Foods Recalls Sausage Due to Foreign Matter

    Kent Quality Foods is recalling ready-to-eat Polish sausage products due to possible contamination with flexible pink rubber pieces.

    Product
    Kent Quality Foods Inc. — Kent Quality Foods, Inc. Recalls Ready-To-Eat Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·19V561000·2019-07-26

    Moto Guzzi and Aprilia Motorcycles Recalled for Front Brake Master Cylinder Defect

    Piaggio is recalling specific Moto Guzzi and Aprilia motorcycles because a front brake master cylinder defect may cause unexpected slowing or stopping without warning to following traffic.

    Product
    MOTO GUZZI — MOTO GUZZI, APRILIA CALIFORNIA, DORSODURO, ELDORADO, AUDACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·19175·2019-07-25

    Cannondale CAADX Bicycles Recalled Due to Fork Breakage and Fatality Risk

    Cycling Sports Group is recalling 2013-2016 Cannondale CAADX bicycles because the fork can break, posing a fall hazard. One fatality and seven serious injuries have been reported.

    Product
    2013 through 2016 Cannondale CAADX cyclocross bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·078-2019·2019-07-25

    Home Market Foods Recalls Frozen Meatballs for Undeclared Allergens

    Home Market Foods is recalling approximately 53,217 pounds of frozen ready-to-eat beef and pork meatballs because they contain undeclared milk and wheat allergens.

    Product
    Home Market Foods, Inc. — Home Market Foods, Inc. Recalls Frozen Ready-To-Eat Beef and Pork Meatball Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1560-2019·2019-07-24

    Pure Ground Ingredients Organic Fennel Seed Recalled for Salmonella

    Pure Ground Ingredients is recalling Organic Fennel Seed in 40 lb. bags because testing found the product positive for Salmonella.

    Product
    Pure Ground Ingredients Organic Fennel Seed, Tea bag Cut 40 lb. bags; Item # FENO-TC Processed and Packaged by: Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1559-2019·2019-07-24

    Pure Ground Ingredients Organic Fennel Seed Recalled for Salmonella

    Pure Ground Ingredients is recalling 35 lb. bags of Organic Fennel Seed because testing found the product positive for Salmonella.

    Product
    Pure Ground Ingredients Organic Fennel Seed, Ground 35 lb. bags Item # FENO-GR Processed and Packaged by: Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-1912-2019·2019-07-24

    Teleflex Neonatal Breathing Circuit Recall Due to Cracked Adaptors

    Teleflex is recalling 20 units of Neonatal ConchaSmart Breathing Circuits due to reported cracks on swivel wye adaptors observed prior to use.

    Product
    Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated Limb and ConchaSmart Column: a) REF 870-07KIT b) REF 870-09KIT Product Usage: The Neonatal ConchaSmart breathing circuits are intended to deliver humidified breathing gases for administration to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1555-2019·2019-07-24

    Shelton Farms Recalls Raw Jalapenos for Salmonella Risk

    Shelton Farms is recalling raw fresh whole jalapenos due to a potential Salmonella contamination. The product was distributed to food service and retail locations in Michigan and Indiana.

    Product
    Raw fresh whole jalapeno, ambient Non-descript 10# cardboard box. Sold as 10lb unit or by the pound.
    Category
    Food
    Distribution
    2 states