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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18976–19000 of 39605

  • SevereFDA (Drugs)·D-0225-2018·2018-01-24

    Rugby Diocto Syrup Recalled for Microbial Contamination

    Pharmatech LLC is recalling Rugby Diocto Syrup due to microbial contamination, including the presence of yeast and potential B. cepacia.

    Product
    Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1001-85, Manufactured by PharmaTech LLC, Davie, FL
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0224-2018·2018-01-24

    Rugby Diocto Liquid Recalled for Microbial Contamination

    PharmaTech LLC is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85, Manufactured by PharmaTech LLC, Davie, FL
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0221-2018·2018-01-24

    Pharmedium Recalls Superpotent Phenylephrine Syringes Nationwide

    Pharmedium Services is voluntarily recalling 2,390 syringes of Phenylephrine HCL 100 mcg/mL due to a superpotent drug classification.

    Product
    Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in 0.9% Sodium Chloride 10 mL syringes, PharMEDium Services, LLC 913 N Davis Ave Cleveland, MS, NDC 71019-263-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0572-2018·2018-01-24

    Gel Spice Recalls Beef Bouillon Cubes for Undeclared Soy and Wheat

    Gel Spice Co, Inc. is recalling beef flavored bouillon cubes because they contain undeclared soy and wheat allergens.

    Product
    Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-0580-2018·2018-01-24

    Polly Ann Mango Ice Cream Bar Recalled for Undeclared Milk Allergen

    California Popsicle, Inc. is recalling Polly Ann Mango Ice Cream Bars due to an undeclared milk allergen. The product was distributed in New York, California, and Canada.

    Product
    Polly Ann Mango Ice Cream Bar 4 BARS-2.5 FL. OZ. (75mL) TOTAL 10 FL. OZ. (300mL) UPC 7 00730 28866 1
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0573-2018·2018-01-24

    Gel Spice Recalls Beef Bouillon Cubes for Undeclared Soy and Wheat

    Gel Spice Co, Inc. is recalling beef flavored bouillon cubes because they contain undeclared soy and wheat allergens.

    Product
    Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Drugs)·D-0226-2018·2018-01-24

    Rugby Senexon Liquid Recalled for Microbial Contamination

    Pharmatech LLC is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59 ; ALSO LABELED AS Major Senna Syrup Natural Vegetable…
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0353-2018·2018-01-24

    Zoll LifeVest Wearable Defibrillator Recalled for Defibrillation Shock Failure Risk

    Zoll Manufacturing Corp. is recalling 33,670 LifeVest Wearable Defibrillators due to an incorrect service code that may prevent the device from detecting critical defects, potentially leading to defibrillation shock failure.

    Product
    LifeVest Wearable Defibrillator Model 4000, Product Number 10A0988-A01. The LifeVest system is indicated for patients 18 years of age and older who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·005-2018·2018-01-23

    Perdue Recalls Chicken Fritters Due to Undeclared Egg Allergen

    Perdue Foods is recalling approximately 530 pounds of chicken breast tenderloin fritters because they contain egg whites, an undeclared allergen.

    Product
    Perdue Foods LLC — Perdue Foods LLC Recalls Chicken Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·18V064000·2018-01-22

    Suzuki Recalls 2017-2018 GSX-R1000 Motorcycles for Chain Break Risk

    Suzuki is recalling 2017-2018 GSX-R1000 motorcycles because a gear shift error can cause the drive chain to break, leading to power loss and crash risk.

    Product
    SUZUKI — SUZUKI GSX-R1000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·004-2018·2018-01-18

    Café Spice Recalls Chicken Salad Products Due to Undeclared Milk Allergen

    Café Spice GCT Inc. is recalling ready-to-eat chicken salad products because they contain milk, an undeclared allergen, and are mislabeled as chicken wraps.

    Product
    CAFE SPICE LLC — Café Spice GCT Inc., Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0566-2018·2018-01-17

    Nodine's Smokehouse Recalls Smoked Salmon Due to Listeria Risk

    Nodine's Smokehouse Inc. is recalling smoked salmon packages nationwide due to potential Listeria monocytogenes contamination.

    Product
    Smoked salmon in 1.5 oz. and 8 oz. packages
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0564-2018·2018-01-17

    Haldiram's Fresh Paneer Recalled Due to Listeria monocytogenes Contamination

    Kotecha Brothers LLC is recalling Haldiram's Fresh Paneer after a sample tested positive for Listeria monocytogenes. The product was distributed to Florida consignees.

    Product
    Haldiram's Fresh Paneer Traditional Indian Soft Cottage Cheese, Net Weight 800g (28.2 oz)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0159-2018·2018-01-17

    Smiths Medical Recalls Sterile Eyewash Due to Leaking Containers

    Smiths Medical is recalling 130,740 bottles of Sterile Eyewash because leaking containers may compromise sterility and expose users to infectious agents.

    Product
    Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 16 oz. 12 units per box. Manufactured by Medex Cardio-Pulmonary Inc. d.b.a. Smiths Medical Company, 300 Corporate Woods Pkwy, Vernon Hills. Illinois, USA 60061. Model Number: 32-005585
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Food)·F-0638-2018·2018-01-17

    Jack Brown Produce Recalls Fuji Apples for Listeria Contamination Risk

    Jack Brown Produce is voluntarily recalling Fuji apples due to potential Listeria monocytogenes contamination reported by a supplier.

    Product
    Fuji, whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0617-2018·2018-01-17

    Nyblad Orchards Recalls Honeycrisp Apples Due to Listeria Risk

    Nyblad Orchards is voluntarily recalling Honeycrisp apples due to potential Listeria monocytogenes contamination. The recall covers various package sizes distributed in Michigan.

    Product
    Honey crisp, whole fresh apples, Apple Ridge 5lb, 2-3/4 apples, packaged in red net mesh bags " 3lb, 2-1/2 apples, packaged in poly bags " 2lb, 2-1/2 apples, packaged in poly bags " 45ct individual apples on trays with re-useable plastic container boxes " 50ct…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0639-2018·2018-01-17

    Jack Brown Produce Recalls Golden Delicious Apples Due to Listeria Risk

    Jack Brown Produce is voluntarily recalling Golden Delicious apples due to potential Listeria monocytogenes contamination. The recall affects specific lots distributed in five US states.

    Product
    Golden Delicious whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0559-2018·2018-01-17

    New Seasons Market Macaroni and Cheese Recalled for Undeclared Egg

    New Seasons Market is recalling pre-packaged macaroni and cheese due to undeclared egg. The product was sold in California, Oregon, and Washington.

    Product
    New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese - refrigerated. Product is packaged in aluminum shallow containers with a clear plastic dome lid and sold in two sizes: Small package UPC 252089 203999. Large package UPC 252090 706991. The label is read…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0618-2018·2018-01-17

    Nyblad Orchards Recalls Fuji Apples Due to Listeria Risk

    Nyblad Orchards is voluntarily recalling Fuji apples due to potential Listeria monocytogenes contamination. The recall covers various package sizes distributed in Michigan.

    Product
    Fuji, whole fresh apples, Apple Ridge 5lb, 2-3/4 apples, packaged in red net mesh bags " 3lb, 2-1/2 apples, packaged in poly bags " 2lb, 2-1/2 apples, packaged in poly bags " 45ct individual apples on trays with re-useable plastic container boxes " 50ct, individual…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0293-2018·2018-01-17

    Edwards Certitude Delivery System Recalled for Molding Overflow Defect

    Edwards Lifesciences is recalling 1,730 units of the Certitude Delivery System due to a molding overflow defect that could detach and embolize into patients.

    Product
    Certitude Delivery System and any associated Multipacks Models - 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A Product Usage: The Edwards Certitude Delivery System is used for delivery of the Edwards SAPIEN 3 transcatheter heart valve (THV), typically during a transapical (TA)…
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0208-2018·2018-01-17

    Teva Recalls Moexipril Hydrochloride Tablets Due to Impurity Test Failure

    Teva Pharmaceuticals is recalling specific bottles of Moexipril Hydrochloride and Hydrochlorothiazide tablets because routine stability testing found high levels of a degradation impurity.

    Product
    Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5213-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0640-2018·2018-01-17

    Jack Brown Produce Recalls Apples Due to Listeria Risk

    Jack Brown Produce is voluntarily recalling multiple varieties of apples because they may be contaminated with Listeria monocytogenes.

    Product
    Golden Del., Gala, Fuji, Honey Crisp; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0619-2018·2018-01-17

    Nyblad Orchards Recalls Fresh Apples Due to Listeria Risk

    Nyblad Orchards is voluntarily recalling multiple varieties of fresh apples due to potential contamination with Listeria monocytogenes.

    Product
    Gala, Fuji., honey crisp, golden delicious whole fresh apples, Apple Ridge 5lb, 2-3/4 apples, packaged in red net mesh bags " 3lb, 2-1/2 apples, packaged in poly bags " 2lb, 2-1/2 apples, packaged in poly bags " 45ct individual apples on trays with re-useable plastic…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0212-2018·2018-01-17

    Pfizer Recalls Atorvastatin Tablets Due to Microbial Contamination

    Pfizer is recalling specific export-only batches of atorvastatin calcium tablets due to microbial contamination. No product was distributed in the United States.

    Product
    FOR EXPORT ONLY Atorvastatin calcium Film-Coated Tablets a) 80 mg SMT Tabs Bulk, b) 40 mg SMT G EP PR KR, c) 20 mg SMT G EP PR, d) 20 mg SMT G EP PR KR, FOR MANUFACTURING, PROCESSING OR REPACKAGING
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0157-2018·2018-01-17

    Smiths Medical Recalls Sterile Eyewash Due to Leaking Containers

    Smiths Medical is recalling 29,232 bottles of Sterile Eyewash because leaking containers may compromise sterility and expose users to infectious agents.

    Product
    Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 1 oz. 144 units per box. Manufactured by Medex Cardio-Pulmonary Inc. d.b.a. Smiths Medical Company, 300 Corporate Woods Pkwy, Vernon Hills. Illinois, USA 60061 Model Number: 32-005582.
    Category
    Medical Device
    Distribution
    2 states