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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22626–22650 of 39699

  • SevereFDA (Food)·F-0200-2017·2016-10-26

    QualiTech Recalls Jalapeno Product Due to Potential E. coli O121 Contamination

    QualiTech is recalling 3,200 lbs of FE Jalapeno 709 due to potential E. coli O121 contamination. The product was distributed in 10 US states and Canada.

    Product
    FE Jalapeno 709, Product Code 22709. 50 lb corrugated case with polyliner. Manufactured by: Quali Tech, 318 Hazel tine Drive, Chasma, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0177-2017·2016-10-26

    Dollar General Recalls Mold-Contaminated Soft Baked Chocolate Brownie Cookies

    Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.

    Product
    Cookies Bergen, Soft Baked Chocolate Brownie Cookies, NET WEIGHT: 4.44 OZ (126g), Produced by P.W. Sponmet Sp.l., Poland
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0221-2017·2016-10-26

    Fresh From Texas Recalls HEB Fruit Medley Due to Listeria Risk

    Fresh From Texas Inc. is recalling HEB Ready Fresh Go Fresh Fruit Medley 7 oz. packages due to potential Listeria monocytogenes contamination.

    Product
    HEB Ready Fresh Go Fresh Fruit Medley 7 oz. UPC 4122002402 packaged in clear plastic tray
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0194-2017·2016-10-26

    QualiTech Recalls Jalapeno Product Due to Potential E. coli O121 Presence

    QualiTech is recalling FE Jalapeno 321A because a supplier reported the potential presence of E. coli O121 bacteria.

    Product
    FE Jalapeno 321A, Product Code 22321A. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0231-2017·2016-10-26

    Windstone Medical Recalls Major General Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Major General Pack, Kit number 002645-11 and 002645-12 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0157-2017·2016-10-26

    Union Bagel Shop Recalls Sourdough Bagels Due to Undeclared Wheat

    Union Bagel Shop is recalling sourdough bagels because they contain undeclared wheat. The products were sold at one retail store in Grande, Oregon.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Sour Dough: Flour, Filtered Water, Olive Oil, Organic Shortening, Malt, Sugar, Sea Salt, Sourdough Start.***" 2 bagels per package - plastic bag with twist tie.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0260-2017·2016-10-26

    Windstone Medical Packaging Recalls Peri Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Peri Kit, Kit number PSS1037 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0054-2017·2016-10-26

    Vascular Solutions Recalls Twin-Pass RX Dual Access Catheters Due to Manufacturing Defect

    Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.

    Product
    Vascular Solutions Twin-Pass RX Dual Access Catheter, model 5210. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0215-2017·2016-10-26

    Fresh From Texas Recalls HEB Sliced Red Apples With Caramel Dip

    Fresh From Texas Inc. is recalling HEB Ready Fresh Go Sliced Red Apples With Caramel Dip due to potential Listeria monocytogenes contamination.

    Product
    HEB Ready Fresh Go Sliced Red Apples With Caramel Dip 16 oz UPC 4122079830 packaged in clear plastic bag
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0191-2017·2016-10-26

    QualiTech Dry Blueberry and Strawberry Blend Recalled for E. coli O121 Risk

    QualiTech is recalling 40,080 lbs of dry blueberry and strawberry blend due to potential E. coli O121 contamination.

    Product
    FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0141-2017·2016-10-26

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.

    Product
    Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0274-2017·2016-10-26

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.

    Product
    Taymour GYN Pack, Kit number PSS2642 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0053-2017·2016-10-26

    Vascular Solutions Recalls Twin-Pass Catheters Due to Manufacturing Material

    Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the tip or in the distal lumen.

    Product
    Vascular Solutions Twin-Pass Dual Access Catheter, models 5200, 5210, and 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0189-2017·2016-10-26

    Birdy 3 in 1 Coffee Mix Recalled for Undeclared Milk Allergen

    Food Gusto, Inc. is recalling Birdy 3 in 1 Robusta Coffee Mix because it may contain undeclared milk and has unclear nutritional labeling.

    Product
    Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed plastic bag, Product of Thailand, UPC 8850250007425
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0105-2017·2016-10-26

    Arbor Pharmaceuticals Recalls Cetylev Tablets Due to Defective Blister Packaging

    Arbor Pharmaceuticals is recalling Cetylev (acetylcysteine) effervescent tablets because incomplete seals on the blister packaging allow moisture to enter, causing the tablets to swell.

    Product
    Cetylev (acetylcysteine) effervescent tablets for oral solution, 500 mg, Rx Only, 20 tablets per carton (ten 2 count blister packs), Distributed by Arbor Pharmaceuticals, LLC Atlanta, GA 30328, NDC 24338-700-10.
    Category
    Drug
    Distribution
    14 states
  • SevereNHTSA·16V777000·2016-10-26

    Ford Recalls 2010-2012 Escape and 2010-2011 Mariner for Fuel Leak Risk

    Ford is recalling specific 2010-2012 Escape and 2010-2011 Mariner vehicles because a cracked fuel delivery module may cause a fuel leak, increasing the risk of fire.

    Product
    FORD — FORD, MERCURY ESCAPE, MARINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0212-2017·2016-10-26

    Del Monte Recalls Cut Green Beans Due to Crawfish Parts

    Del Monte is recalling cut green beans and field peas with snaps due to a customer complaint of finding crawfish parts in the product.

    Product
    Cut Green Beans packed under brand names of: Allens Cut Green Beans (Ejotes Cortados Lago Azul) Blue Lake . Allens Cracker Barrel Label (Both labels have same UPC # - different sodium content - 140 mg for Allens Cut Green Beans and 250 for Cracker Barrel label Peso Neto…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Food)·F-0208-2017·2016-10-26

    QualiTech Recalls PE Blueberries Due to Potential E. coli O121 Contamination

    QualiTech is recalling 176,900 lbs of PE Blueberries due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.

    Product
    PE Blueberry, Product Code 27136. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0005-2017·2016-10-26

    Heartware Ventricular Assist System Controller Recall for Loose Connector Ports

    Heartware, Inc. is recalling Ventricular Assist System Controllers due to loose connector ports. The recall affects 4,235 units worldwide, including 7,272 in the U.S.

    Product
    HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HVAD is designed for in-hospital and out-of-hospital settings…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0213-2017·2016-10-26

    Del Monte Recalls Field Peas and Green Beans Due to Crawfish Parts

    Del Monte is recalling approximately 15,000 cases of canned field peas and green beans after a customer complaint reported finding crawfish parts in the product.

    Product
    Allens East Texas Fair Brand, Tiny Tender Field Peas with snaps; NET.WT. 6 lbs. 15 oz.. (3.15kg) UPC 0 34700 623214 8 Distributed by Sager Creek Vegetable Company, Siloam Springs, AR 72761-0250 USA; UPC 0 34700 63213 1
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-0055-2017·2016-10-26

    Vascular Solutions Recalls Twin-Pass Dual Access Catheters Due to Manufacturing Residue

    Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.

    Product
    Vascular Solutions Twin-Pass .023" Dual Access Catheter, model 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V778000·2016-10-26

    Ford Recalls 2017 F-Series Trucks Due to Fuel Leak Fire Risk

    Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.

    Product
    FORD — FORD F-450 SD, F-550 SD, F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0218-2017·2016-10-26

    Fresh From Texas Recalls Deluxe Fruit Tray for Listeria Risk

    Fresh From Texas Inc. is recalling 18,392 units of Deluxe Fruit Tray 52 oz. due to potential Listeria monocytogenes contamination.

    Product
    Deluxe Fruit Tray 52 oz. UPC 427979661 packaged in clear plastic round container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0106-2017·2016-10-26

    Dream Body Extreme Gold Recalled for Undeclared Sibutramine

    Dream Body Weight Loss is recalling Dream Body Extreme Gold capsules because they contain undeclared sibutramine and were marketed without FDA approval.

    Product
    Dream Body Extreme Gold 800 mg 30 capsules in a plastic screw on top bottle
    Category
    Drug
    Distribution
    0 states