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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31001–31025 of 39756

  • SevereNHTSA·14E037000·2014-07-10

    Airtex E84070 Replacement Fuel Pumps Recalled for Leak Risk

    UCI-Fram Group is recalling Airtex E84070 replacement fuel pumps shipped between December 2013 and June 2014 due to a seal defect that may cause fluid leaks and increase fire risk.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2081-2014·2014-07-09

    Rome Packing Recalls Jonah Crab Meat Contaminated with Listeria

    Rome Packing Co. is recalling 300 lbs of Ocean's Catch Jonah Crab Minced Meat contaminated with Listeria monocytogenes. The product was distributed in six states.

    Product
    Ocean's Catch Jonah Crab Minced Meat Crabmeat , Net WT. 10 lb. plastic bag
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-2079-2014·2014-07-09

    Rome Packing Recalls Ocean's Catch Crabmeat Due to Listeria Contamination

    Rome Packing Co., Inc. is recalling Ocean's Catch Ready-to-Eat Fresh Hand Picked Crabmeat because it is contaminated with Listeria monocytogenes.

    Product
    Ocean's Catch RTE Fresh Hand Picked Crabmeat , Net WT. 6 oz. plastic container Ingredients; Contains Jonah Crab Meat
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-2080-2014·2014-07-09

    Rome Packing Recalls Jonah Crab Meat Due to Listeria Contamination

    Rome Packing Co. is recalling Ocean's Catch Jonah Crab Meat contaminated with Listeria monocytogenes. Consumers should check lot numbers and discard or return affected products.

    Product
    Ocean's Catch RTE All Natural Jonah Crab Combo Meat Fresh Hand Picked Crabmeat , Net WT. 8 oz. and 16 oz. plastic container Ingredients; Contains Jonah Rock Crab Meat, Salt
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1923-2014·2014-07-09

    Medtronic Duet External Drainage System Tubing Disconnection Recall

    Medtronic Neurosurgery is recalling Duet External Drainage and Monitoring Systems because the patient line tubing may become disconnected from the stopcock.

    Product
    Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Catheter, Catalog No. 46916. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-2056-2014·2014-07-09

    Whole Foods Recalls Fresh Wild Gulf Amberjack Due to Illness Complaints

    Whole Foods Market South Seafood Distribution is recalling fresh wild Gulf Amberjack in Georgia after receiving complaints of illness from consumers.

    Product
    Fresh Wild Gulf Amberjack (Whole, Fillet and Portion)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2057-2014·2014-07-09

    Lao Thai Nam Salted Fish Recalled for Botulism Risk

    Lao Thai Nam Corporation is recalling 120 packs of Number One Sompa Salted Fish due to potential Clostridium botulinum contamination. The product was distributed in Texas.

    Product
    Lao Thai Nam Number One Sompa Salted Fish, Net Wt 7 oz. (198 g), Produced by Lao Thai Nam, 4444 W. Illinois Ave., Ste 400a, Dallas, TX 75211, UPC 8 84332 00019 4
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2068-2014·2014-07-09

    Rite Aid Recalls Thrifty Mint 'N' Chip Ice Cream Due to Undeclared Pistachio

    Rite Aid is recalling 560 pints of Thrifty Mint 'N' Chip ice cream because pistachio was inadvertently packed into the containers without being declared on the label.

    Product
    waxed paperboard int container of frozen ice cream labeled Thrifty Ice Cream Mint 'N' Chip 1 Pint (16 Fl. OZ.) Bottom of container Expiration Date: October 28 2015 Lot #24273 Back of container UPC 1182264327
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1920-2014·2014-07-09

    Medtronic Duet External Drainage System Tubing Disconnection Recall

    Medtronic Neurosurgery is recalling Duet External Drainage and Monitoring Systems because the patient line tubing may disconnect from the stopcock.

    Product
    Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Catalog No. 46913. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar subarachnoid…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1978-2014·2014-07-09

    Stryker Triathlon Patella Inserter Recalled for Instrument Fracture Risk

    Stryker Howmedica Osteonics is recalling 22 units of the Triathlon Tritanium Patella Inserter because the instrument may fracture during implantation.

    Product
    Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the Tritanium Knee System Instrument Set. It is used to implant the Tritanium Patella after the patellar bone has been prepared using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1985-2014·2014-07-09

    Siemens Mobilett XP X-ray System Recalled for Fire Hazard

    Siemens is recalling 10 Mobilett XP Digital Mobile X-ray Systems due to a potential fire hazard from Lithium-Ion batteries installed between October 2010 and April 2011.

    Product
    Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Mobilett XP and Mobilett XP Hybrid are radiographic systems designed for use in wards, intensive care, and premature birth-wards, pediatric and emergency departments, operating theatres as well as the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1922-2014·2014-07-09

    Medtronic Duet External Drainage System Tubing Disconnection Recall

    Medtronic Neurosurgery is recalling Duet External Drainage and Monitoring Systems because the patient line tubing may become disconnected from the stopcock.

    Product
    Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Catheter, Catalog No. 46915. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1989-2014·2014-07-09

    GE Healthcare Recalls Revolution XR/d X-ray Systems Due to Collimator Fall Risk

    GE Healthcare is recalling Revolution XR/d digital radiographic systems because a collimator installation error during maintenance could cause the device to fall and injure patients.

    Product
    GE Healthcare, Revolution XR/d. Revolution XR/d Intended Use: The Revolution XR/d Digital Radiographic imaging system is indicated for use in generating radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in all general purpose…
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1948-2014·2014-07-09

    Ventlab Manual Resuscitator Bags Recalled Due to Valve Defect

    Ventlab LLC is recalling 251,384 manual resuscitator bags because a defective pop-off valve may prevent air delivery during emergency resuscitation.

    Product
    Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT5000, BVM700, CPRM1000, CPRM2000, CPRM3000, PRO-1900, PRO-1000, PRO-2000, SC7000, SC8000, SC8020, SC8120, SC9000, SS3200, VN2000, VN3000, VN4000, VN5000, VT1000 , VN2102, VN2002.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2053-2014·2014-07-09

    Baptista's Bakery Recalls Gluten-Free Crackers Due to Salmonella Risk

    Baptista's Bakery is recalling specific lots of Rosemary & Olive Oil Gluten Free Snack Crackers because a seasoning supplier's blend may be contaminated with Salmonella.

    Product
    Rosemary & Olive Oil Gluten Free Snack Crackers sold under the following brand names and sizes: 1. glutino, Net Wt. 4.25 oz (120g) UPC 78523-03861; 2. glutino, 2 count 10 oz bags, Net Wt. 20 oz (566 g) UPC 78523-03863; 3. Aldi's brand live G free, Net Wt. 4.25 oz (120g)…
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-1921-2014·2014-07-09

    Medtronic Duet External Drainage System Tubing Disconnection Recall

    Medtronic is recalling Duet External Drainage and Monitoring Systems because the patient line tubing may disconnect from the stopcock.

    Product
    Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Catalog No. 46914. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar subarachnoid…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1959-2014·2014-07-09

    Atrium Express Dry Seal Chest Drain Recall Due to Leaking Risk

    Atrium Medical Corporation is recalling 1,170 units of the Express Dry Seal Chest Drain ATS Blood Recovery because the tubing may leak or disconnect.

    Product
    Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-1924-2014·2014-07-09

    Medtronic Duet External Drainage System Tubing Disconnection Recall

    Medtronic Neurosurgery is recalling Duet External Drainage and Monitoring Systems because the patient line tubing may become disconnected from the stopcock.

    Product
    Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, Catalog No. 46917. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1988-2014·2014-07-09

    GE Healthcare Recalls Proteus XR/a X-ray Systems Due to Collimator Fall Risk

    GE Healthcare is recalling Proteus XR/a and Revolution XR/d X-ray systems due to a collimator installation error that caused a serious patient injury.

    Product
    GE Healthcare, Proteus XR/a. Proteus XR/a Intended Use: Is intended for use in generating radiographic images of human anatomy in all general purpose diagnostic procedures. This device is not intended for mammographic applications.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1991-2014·2014-07-09

    Siemens Recalls ADVIA Centaur TnI-Ultra Assay Kits Due to Reagent Appearance

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur TnI-Ultra assay kits because a darker solid phase reagent in some lots may lead to incorrect test results.

    Product
    ADVIA Centaur¿ Systems TnI-Ultra assay; Catalog Number 02789602 (100 tests), SMN 10317708 and 02790309 (500 tests), SMN 10317790
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1981-2014·2014-07-09

    Vascular Solutions Recalls Langston Dual Lumen Catheters Due to Separation Risk

    Vascular Solutions is recalling Langston Dual Lumen Catheters because the inner catheter may separate from the hub during use, potentially requiring intervention to prevent injury.

    Product
    Langston Dual Lumen Catheters, 6Fr, REF 5550 and 5540. The Vascular Solutions Langston Dual Lumen Pressure Monitoring catheter is used as a pressure measurement catheter and for delivery of contrast media during angiographic studies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2078-2014·2014-07-09

    Dole Garden Soup Recalled for Undeclared Milk Allergen

    Dole Packaged Foods is recalling Roasted Garlic Tomato Basil soup because it contains undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Dole Garden Soup "Roasted Garlic Tomato Basil", Net Wt. 26 oz. (1lb 10oz) 737 g, UPC 3890002404, 6 units/case
    Category
    Food
    Distribution
    4 states