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

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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

34076–34100 of 39756

  • SevereFDA (Devices)·Z-1858-2013·2013-08-14

    Hospira Recalls Y-Type Blood Sets Due to Potential Bag Puncture

    Hospira Inc. is recalling 3,600 units of Y-Type Blood Sets because the piercing pin may puncture the outer wall of blood bags during insertion.

    Product
    List No. 14219-28; Y-TYPE BLOOD SET; 200 Micron Filter, Cylinder Pump, CLAVE Y-Site, Non-Vented, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-840-2013·2013-08-14

    AstraZeneca Recalls Merrem I.V. Vials Due to Precipitate Presence

    AstraZeneca is recalling specific lots of Merrem I.V. (meropenem) because of precipitate presence, which may prevent the medication from mixing completely.

    Product
    MERREM I.V. (meropenem for injection), 1 g meropenem equivalent, 30 mL vial, Rx only, Mfd for: AstraZeneca Pharmaceuticals LP, Wilmington, DE by ACS Dobfar SpA Viale Addetta, Tribiano, Milano Italy NDC 0310 0321 30
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1856-2013·2013-08-14

    Hospira Recalls Blood Sets Due to Potential Bag Puncture Risk

    Hospira Inc. is recalling specific blood sets because the piercing pin may puncture the outer wall of blood bags during insertion.

    Product
    List No. 14212-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1850-2013·2013-08-14

    Hospira Recalls Secondary Blood Sets Due to Piercing Pin Defect

    Hospira Inc. is recalling 672 units of secondary blood sets because the piercing pin may puncture the outer wall of blood bags during insertion.

    Product
    List No. 14200-28; SECONDARY BLOOD SET; 200 Micron Filter, 36 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1854-2013·2013-08-14

    Hospira Recalls Blood Sets Due to Potential Puncture of Blood Bags

    Hospira Inc. is recalling 96 units of PLUM BLOOD SETS because the piercing pin may puncture the outer wall of blood bags during insertion.

    Product
    List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, Non-Vented, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-852-2013·2013-08-14

    Apotex Recalls Latanoprost Ophthalmic Solution Due to Sterility Concerns

    Apotex Inc. is recalling Latanoprost Ophthalmic Solution, 0.005%, because it failed a preservative effectiveness test, raising concerns about potential microbial growth.

    Product
    Latanoprost Ophthalmic Solution, 0.005% (125 mcg/2.5 mL), 2.5 mL bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario Canada M9L 1T9; Manufactured for: Apotex Corp., Weston, FL 33326; NDC 60505-0565-1; UPC 3 60505 05651 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1874-2013·2013-08-14

    Iradimed MRidium Dose Reduction System Recall for Infusion Rate Errors

    Iradimed is recalling MRidium 1145 Dose Reduction System kits because they may display incorrect infusion rates, posing a risk of over- or under-infusion.

    Product
    MRidium 1145 Dose Reduction System (DERS) drug library kit. (This is an option for the MRidium 3860+MR Infusion Pump System). The MRidium 3860+MRI Infusion pump are intended for general hospital or clinical use by medical professional whenever it is required to infuse…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·13747·2013-08-14

    John Deere Recalls Compact Utility Tractors Due to ROPS Pin Failure Risk

    John Deere is recalling about 7,000 compact utility tractors because spring locking pins in the rollover protective system can break, posing a risk of serious injury or death.

    Product
    John Deere Compact Utility Tractors
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13748·2013-08-14

    LTD Commodities Recalls Microwave Crisper Pans Due to Fire Hazard

    LTD Commodities is recalling microwave crisper pans because a metal washer can spark, posing a fire hazard. The firm reported 16 incidents involving sparks, flames, or shattered glass.

    Product
    Microwave Crisper Pan with Lids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1853-2013·2013-08-14

    Hospira Blood Sets Recalled Due to Potential Bag Puncture Risk

    Hospira is recalling 240 blood sets because the piercing pin may puncture the outer wall of blood bags during insertion.

    Product
    List No. 14207-28; BLOOD SET; 200 Micron Filter, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1887-2013·2013-08-14

    Cordis OPTEASE Retrieval IVC Filter Recall for Labeling Clarification

    Cordis Corporation is recalling 33,000 units of the OPTEASE Retrieval IVC Filter to provide additional labeling that minimizes the likelihood of implanting the filter backwards.

    Product
    Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and Introduction Kit***(BRITE TIP Catheter Sheath Introducer and Angiographic Vessel Dilator)***Cordis***a Johnson and Johnson Company***ENDOVASCULAR*** Label No.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1835-2013·2013-08-14

    CareFusion Recalls Alaris PC Units Due to Voltage and Communication Issues

    CareFusion is recalling Alaris PC units model 8015 because they operate at incorrect voltage and may lose communication between processors.

    Product
    Alaris PC unit, model 8015, with version 9.12-Keyboard Processor and logic board assembly part number TC10006584. The Alaris PC Unit is the main user interface unit and power supply of the Alaris System, a modular system to be used with Alaris System modules intended for use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-836-2013·2013-08-14

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 0.9% Sodium Chloride Injection, USP, 1000 mL containers due to the presence of small grey/brown brass particulates.

    Product
    0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V356000·2013-08-13

    Kia Recalls 2014 Sorento Vehicles Due to Front Axle Shaft Fracture Risk

    Kia is recalling specific 2014 Sorento vehicles because a manufacturing issue may cause the right front axle shaft to fracture, potentially leading to loss of power or the vehicle rolling away.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V354000·2013-08-12

    Hyundai Recalls Sonata and Azera for Rear Suspension Corrosion Risk

    Hyundai is recalling 2006-2011 Sonata and Azera vehicles in 22 states and D.C. because road salt can corrode the rear crossmember, potentially causing a control arm to detach.

    Product
    HYUNDAI — HYUNDAI AZERA, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V353000·2013-08-12

    Spartan Aerial Fire Vehicles Recalled for Detaching Rotation Interlock Magnets

    Spartan ERV is recalling specific aerial fire vehicles because adhesive on rotation interlock magnets degrades, causing them to detach and potentially leading to vehicle instability and rollover.

    Product
    SPARTAN — SPARTAN RMA 103, RMP 100, RMA 75, TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E043000·2013-08-12

    Airtex Fuel Pumps Recalled for Potential Fire Risk in GM Vehicles

    Airtex is recalling fuel pumps for certain 2004-2008 GM vehicles because an electrical connector may not seal, allowing fuel to escape and increasing fire risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V366000·2013-08-09

    Volvo Recalls 2013-2014 VNL Trucks Due to Driveshaft Failure Risk

    Volvo Trucks North America is recalling 2013-2014 VNL trucks because a weak driveshaft may fail, potentially causing debris on the roadway and increasing crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13260·2013-08-08

    Big Lots Recalls Citronella Tabletop Torches Due to Fire and Burn Hazards

    Big Lots is recalling approximately 30,000 citronella tabletop torches sold nationwide from March to June 2013 because they can flare up and emit burning fuel, posing fire and burn risks.

    Product
    Citronella Tabletop Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1783-2013·2013-08-07

    Lipari Foods Recalls Wholey Shrimp Due to Salmonella Risk

    Lipari Foods is recalling Wholey peeled, cooked shrimp because it may be contaminated with Salmonella, which can cause serious infections in vulnerable populations.

    Product
    WHOLEY Shrimp, Farm Raised, Cooked, Peeled Deveined, Tail on, Ingredients: Shrimp, Salt and Sodium Tripolyphosphate..., ,Net Wt 1 LB (16 oz) , 399103 UPC Number: 094776074556; Product of Indonesia
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1775-2013·2013-08-07

    Hagee Foods Recalls Black Bean Hummus Due to Listeria Risk

    Hagee Foods Inc. is recalling specific varieties of Black Bean Hummus due to potential contamination with Listeria monocytogenes. The products were distributed in Oregon and Washington.

    Product
    Penny's Black Bean Hummus 12 oz has UPC 7 49404 70200 3; Harbor Greens Black Bean Hummus 8 oz has UPC 7 49404 80515 5; Tacoma Boys Black Bean Hummus 8 oz has UPC 7 49404 90515 2.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-828-2013·2013-08-07

    Green Planet Night Bullet Capsules Recalled for Unapproved Active Ingredients

    Green Planet Inc is recalling Night Bullet Capsules because they contain unapproved active ingredients for erectile dysfunction.

    Product
    Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1761-2013·2013-08-07

    El Campestre Seafood Ranchero Recalled for Undeclared Allergens

    El Campestre is recalling Seafood Ranchero because it contains undeclared eggs, soy, wheat, and crab extract.

    Product
    El Campestre Brand Seafood Ranchero. Packaged in 2/5lbs white plastic buckets with lid and handle, into 1/10lbs carton. Labeling reads in part:"SEA FOOD RANCHERO***NET WT..10 LBS***DIST.BY EL CAMPESTRE DIST TEL (562) 505-7247***".
    Category
    Food
    Distribution
    1 state